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nsv7098698

  • Variant Calls:11
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):167,614,082-167,614,082Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):167,614,082-167,614,082Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):167,751,110-167,751,110Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):167,751,114-167,751,114Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):167,751,282-167,751,282Question Mark
    Overlapping variant regions from other studies: 102 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):167,841,491-167,841,491Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):167,860,721-167,860,721Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):167,861,504-167,861,504Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):167,863,917-167,863,917Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):167,863,917-167,863,917Question Mark
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):171,343,838-171,343,838Question Mark
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):171,343,838-171,343,838Question Mark
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):94,084,314-94,084,314Question Mark
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):94,084,322-94,084,322Question Mark
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):121,115,002-121,115,002Question Mark
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):121,115,009-121,115,009Question Mark
    Overlapping variant regions from other studies: 116 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):121,163,303-121,163,303Question Mark
    Overlapping variant regions from other studies: 116 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):121,163,304-121,163,304Question Mark
    Overlapping variant regions from other studies: 78 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):20,821,385-20,821,385Question Mark
    Overlapping variant regions from other studies: 78 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):20,821,390-20,821,390Question Mark
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):20,857,144-20,857,144Question Mark
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):20,857,147-20,857,147Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Submitted genomic167,331,870-167,331,870Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Submitted genomic167,331,870-167,331,870Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Submitted genomic167,468,898-167,468,898Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Submitted genomic167,468,902-167,468,902Question Mark
    Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
    Submitted genomic167,469,070-167,469,070Question Mark
    Overlapping variant regions from other studies: 102 SVs from 18 studies. See in: genome view    
    Submitted genomic167,559,279-167,559,279Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Submitted genomic167,578,509-167,578,509Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Submitted genomic167,579,292-167,579,292Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Submitted genomic167,581,705-167,581,705Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Submitted genomic167,581,705-167,581,705Question Mark
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Submitted genomic171,061,627-171,061,627Question Mark
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Submitted genomic171,061,627-171,061,627Question Mark
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Submitted genomic93,803,158-93,803,158Question Mark
    Overlapping variant regions from other studies: 105 SVs from 32 studies. See in: genome view    
    Submitted genomic93,803,166-93,803,166Question Mark
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Submitted genomic122,874,516-122,874,516Question Mark
    Overlapping variant regions from other studies: 106 SVs from 16 studies. See in: genome view    
    Submitted genomic122,874,523-122,874,523Question Mark
    Overlapping variant regions from other studies: 116 SVs from 22 studies. See in: genome view    
    Submitted genomic122,922,817-122,922,817Question Mark
    Overlapping variant regions from other studies: 116 SVs from 22 studies. See in: genome view    
    Submitted genomic122,922,818-122,922,818Question Mark
    Overlapping variant regions from other studies: 78 SVs from 25 studies. See in: genome view    
    Submitted genomic20,842,931-20,842,931Question Mark
    Overlapping variant regions from other studies: 78 SVs from 25 studies. See in: genome view    
    Submitted genomic20,842,936-20,842,936Question Mark
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Submitted genomic20,878,690-20,878,690Question Mark
    Overlapping variant regions from other studies: 68 SVs from 20 studies. See in: genome view    
    Submitted genomic20,878,693-20,878,693Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,614,082167,614,082+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,614,082167,614,082-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,751,110167,751,110-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,751,114167,751,114+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,751,282167,751,282+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,841,491167,841,491-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,860,721167,860,721+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,861,504167,861,504-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,863,917167,863,917+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3167,863,917167,863,917-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3171,343,838171,343,838+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3171,343,838171,343,838-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr394,084,31494,084,314+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr394,084,32294,084,322-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10121,115,002121,115,002-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10121,115,009121,115,009+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10121,163,303121,163,303-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10121,163,304121,163,304+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,821,38520,821,385+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,821,39020,821,390-
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,857,14420,857,144+
    nsv7098698RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,857,14720,857,147-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,331,870167,331,870+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,331,870167,331,870-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,468,898167,468,898-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,468,902167,468,902+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,469,070167,469,070+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,559,279167,559,279-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,578,509167,578,509+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,579,292167,579,292-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,581,705167,581,705+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3167,581,705167,581,705-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3171,061,627171,061,627+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3171,061,627171,061,627-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr393,803,15893,803,158+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr393,803,16693,803,166-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10122,874,516122,874,516-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10122,874,523122,874,523+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10122,922,817122,922,817-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10122,922,818122,922,818+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1120,842,93120,842,931+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1120,842,93620,842,936-
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1120,878,69020,878,690+
    nsv7098698Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1120,878,69320,878,693-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792485intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792492intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792488interchromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792493intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792489interchromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792491intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792494intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792495interchromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792490interchromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792487intrachromosomal translocationFHU18-275SequencingSequence alignment11
    nssv18792486interchromosomal translocationFHU18-275SequencingSequence alignment11

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792485RemappedPerfectGRCh38.p12First PassNC_000003.12Chr394,084,31494,084,314+
    nssv18792492RemappedPerfectGRCh38.p12First PassNC_000003.12Chr394,084,32294,084,322-
    nssv18792488RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,614,082167,614,082-
    nssv18792493RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,614,082167,614,082+
    nssv18792492RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,751,110167,751,110-
    nssv18792489RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,751,114167,751,114+
    nssv18792491RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,751,282167,751,282+
    nssv18792494RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,841,491167,841,491-
    nssv18792495RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,860,721167,860,721+
    nssv18792491RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,861,504167,861,504-
    nssv18792490RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,863,917167,863,917+
    nssv18792494RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3167,863,917167,863,917-
    nssv18792485RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3171,343,838171,343,838-
    nssv18792493RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3171,343,838171,343,838+
    nssv18792487RemappedPerfectGRCh38.p12First PassNC_000010.11Chr10121,115,002121,115,002-
    nssv18792486RemappedPerfectGRCh38.p12First PassNC_000010.11Chr10121,115,009121,115,009+
    nssv18792487RemappedPerfectGRCh38.p12First PassNC_000010.11Chr10121,163,303121,163,303-
    nssv18792488RemappedPerfectGRCh38.p12First PassNC_000010.11Chr10121,163,304121,163,304+
    nssv18792486RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1120,821,38520,821,385+
    nssv18792490RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1120,821,39020,821,390-
    nssv18792489RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1120,857,14420,857,144+
    nssv18792495RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1120,857,14720,857,147-
    nssv18792485Submitted genomicGRCh37 (hg19)NC_000003.11Chr393,803,15893,803,158+
    nssv18792492Submitted genomicGRCh37 (hg19)NC_000003.11Chr393,803,16693,803,166-
    nssv18792488Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,331,870167,331,870-
    nssv18792493Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,331,870167,331,870+
    nssv18792492Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,468,898167,468,898-
    nssv18792489Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,468,902167,468,902+
    nssv18792491Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,469,070167,469,070+
    nssv18792494Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,559,279167,559,279-
    nssv18792495Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,578,509167,578,509+
    nssv18792491Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,579,292167,579,292-
    nssv18792490Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,581,705167,581,705+
    nssv18792494Submitted genomicGRCh37 (hg19)NC_000003.11Chr3167,581,705167,581,705-
    nssv18792485Submitted genomicGRCh37 (hg19)NC_000003.11Chr3171,061,627171,061,627-
    nssv18792493Submitted genomicGRCh37 (hg19)NC_000003.11Chr3171,061,627171,061,627+
    nssv18792487Submitted genomicGRCh37 (hg19)NC_000010.10Chr10122,874,516122,874,516-
    nssv18792486Submitted genomicGRCh37 (hg19)NC_000010.10Chr10122,874,523122,874,523+
    nssv18792487Submitted genomicGRCh37 (hg19)NC_000010.10Chr10122,922,817122,922,817-
    nssv18792488Submitted genomicGRCh37 (hg19)NC_000010.10Chr10122,922,818122,922,818+
    nssv18792486Submitted genomicGRCh37 (hg19)NC_000011.9Chr1120,842,93120,842,931+
    nssv18792490Submitted genomicGRCh37 (hg19)NC_000011.9Chr1120,842,93620,842,936-
    nssv18792489Submitted genomicGRCh37 (hg19)NC_000011.9Chr1120,878,69020,878,690+
    nssv18792495Submitted genomicGRCh37 (hg19)NC_000011.9Chr1120,878,69320,878,693-

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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