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nsv7098709

  • Variant Calls:10
  • 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: 149 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):137,740,158-137,740,158Question Mark
    Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):137,740,158-137,740,158Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):228,275,730-228,275,730Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):228,275,732-228,275,732Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):229,135,289-229,135,289Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):229,135,292-229,135,292Question Mark
    Overlapping variant regions from other studies: 196 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):229,948,571-229,948,571Question Mark
    Overlapping variant regions from other studies: 196 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):229,948,574-229,948,574Question Mark
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):231,705,911-231,705,911Question Mark
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):231,705,911-231,705,911Question Mark
    Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):231,713,973-231,713,973Question Mark
    Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):231,713,973-231,713,973Question Mark
    Overlapping variant regions from other studies: 280 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):232,367,019-232,367,019Question Mark
    Overlapping variant regions from other studies: 282 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):232,367,161-232,367,161Question Mark
    Overlapping variant regions from other studies: 72 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):156,218,540-156,218,540Question Mark
    Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):166,293,601-166,293,601Question Mark
    Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):77,034,516-77,034,516Question Mark
    Overlapping variant regions from other studies: 73 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):77,034,517-77,034,517Question Mark
    Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):95,297,050-95,297,050Question Mark
    Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):95,297,057-95,297,057Question Mark
    Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view    
    Submitted genomic138,497,728-138,497,728Question Mark
    Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view    
    Submitted genomic138,497,728-138,497,728Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Submitted genomic229,140,446-229,140,446Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Submitted genomic229,140,448-229,140,448Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Submitted genomic230,000,005-230,000,005Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Submitted genomic230,000,008-230,000,008Question Mark
    Overlapping variant regions from other studies: 196 SVs from 30 studies. See in: genome view    
    Submitted genomic230,813,287-230,813,287Question Mark
    Overlapping variant regions from other studies: 196 SVs from 30 studies. See in: genome view    
    Submitted genomic230,813,290-230,813,290Question Mark
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Submitted genomic232,570,621-232,570,621Question Mark
    Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
    Submitted genomic232,570,621-232,570,621Question Mark
    Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view    
    Submitted genomic232,578,683-232,578,683Question Mark
    Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view    
    Submitted genomic232,578,683-232,578,683Question Mark
    Overlapping variant regions from other studies: 280 SVs from 51 studies. See in: genome view    
    Submitted genomic233,231,729-233,231,729Question Mark
    Overlapping variant regions from other studies: 282 SVs from 50 studies. See in: genome view    
    Submitted genomic233,231,871-233,231,871Question Mark
    Overlapping variant regions from other studies: 72 SVs from 19 studies. See in: genome view    
    Submitted genomic155,645,550-155,645,550Question Mark
    Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
    Submitted genomic165,720,606-165,720,606Question Mark
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Submitted genomic76,745,560-76,745,560Question Mark
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Submitted genomic76,745,561-76,745,561Question Mark
    Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
    Submitted genomic95,030,214-95,030,214Question Mark
    Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
    Submitted genomic95,030,221-95,030,221Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2137,740,158137,740,158+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2137,740,158137,740,158-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2228,275,730228,275,730+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2228,275,732228,275,732-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2229,135,289229,135,289-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2229,135,292229,135,292+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2229,948,571229,948,571-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2229,948,574229,948,574+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2231,705,911231,705,911+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2231,705,911231,705,911-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2231,713,973231,713,973+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2231,713,973231,713,973-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2232,367,019232,367,019+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2232,367,161232,367,161+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5156,218,540156,218,540+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5166,293,601166,293,601-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1177,034,51677,034,516-
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1177,034,51777,034,517+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1195,297,05095,297,050+
    nsv7098709RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1195,297,05795,297,057-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2138,497,728138,497,728+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2138,497,728138,497,728-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2229,140,446229,140,446+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2229,140,448229,140,448-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2230,000,005230,000,005-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2230,000,008230,000,008+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2230,813,287230,813,287-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2230,813,290230,813,290+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2232,570,621232,570,621+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2232,570,621232,570,621-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2232,578,683232,578,683+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2232,578,683232,578,683-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2233,231,729233,231,729+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2233,231,871233,231,871+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5155,645,550155,645,550+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5165,720,606165,720,606-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1176,745,56076,745,560-
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1176,745,56176,745,561+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1195,030,21495,030,214+
    nsv7098709Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1195,030,22195,030,221-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792441intrachromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792448intrachromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792449intrachromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792446interchromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792445interchromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792447interchromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792442intrachromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792443intrachromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792450interchromosomal translocationFHU17-112SequencingSequence alignment10
    nssv18792444intrachromosomal translocationFHU17-112SequencingSequence alignment10

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792441RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2137,740,158137,740,158+
    nssv18792448RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2137,740,158137,740,158-
    nssv18792449RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2228,275,730228,275,730+
    nssv18792446RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2228,275,732228,275,732-
    nssv18792448RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2229,135,289229,135,289-
    nssv18792445RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2229,135,292229,135,292+
    nssv18792441RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2229,948,571229,948,571-
    nssv18792447RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2229,948,574229,948,574+
    nssv18792442RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2231,705,911231,705,911+
    nssv18792443RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2231,705,911231,705,911-
    nssv18792442RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2231,713,973231,713,973+
    nssv18792450RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2231,713,973231,713,973-
    nssv18792449RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2232,367,019232,367,019+
    nssv18792443RemappedPerfectGRCh38.p12First PassNC_000002.12Chr2232,367,161232,367,161+
    nssv18792444RemappedPerfectGRCh38.p12First PassNC_000005.10Chr5156,218,540156,218,540+
    nssv18792444RemappedPerfectGRCh38.p12First PassNC_000005.10Chr5166,293,601166,293,601-
    nssv18792447RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1177,034,51677,034,516-
    nssv18792445RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1177,034,51777,034,517+
    nssv18792446RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1195,297,05095,297,050+
    nssv18792450RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1195,297,05795,297,057-
    nssv18792441Submitted genomicGRCh37 (hg19)NC_000002.11Chr2138,497,728138,497,728+
    nssv18792448Submitted genomicGRCh37 (hg19)NC_000002.11Chr2138,497,728138,497,728-
    nssv18792449Submitted genomicGRCh37 (hg19)NC_000002.11Chr2229,140,446229,140,446+
    nssv18792446Submitted genomicGRCh37 (hg19)NC_000002.11Chr2229,140,448229,140,448-
    nssv18792448Submitted genomicGRCh37 (hg19)NC_000002.11Chr2230,000,005230,000,005-
    nssv18792445Submitted genomicGRCh37 (hg19)NC_000002.11Chr2230,000,008230,000,008+
    nssv18792441Submitted genomicGRCh37 (hg19)NC_000002.11Chr2230,813,287230,813,287-
    nssv18792447Submitted genomicGRCh37 (hg19)NC_000002.11Chr2230,813,290230,813,290+
    nssv18792442Submitted genomicGRCh37 (hg19)NC_000002.11Chr2232,570,621232,570,621+
    nssv18792443Submitted genomicGRCh37 (hg19)NC_000002.11Chr2232,570,621232,570,621-
    nssv18792442Submitted genomicGRCh37 (hg19)NC_000002.11Chr2232,578,683232,578,683+
    nssv18792450Submitted genomicGRCh37 (hg19)NC_000002.11Chr2232,578,683232,578,683-
    nssv18792449Submitted genomicGRCh37 (hg19)NC_000002.11Chr2233,231,729233,231,729+
    nssv18792443Submitted genomicGRCh37 (hg19)NC_000002.11Chr2233,231,871233,231,871+
    nssv18792444Submitted genomicGRCh37 (hg19)NC_000005.9Chr5155,645,550155,645,550+
    nssv18792444Submitted genomicGRCh37 (hg19)NC_000005.9Chr5165,720,606165,720,606-
    nssv18792447Submitted genomicGRCh37 (hg19)NC_000011.9Chr1176,745,56076,745,560-
    nssv18792445Submitted genomicGRCh37 (hg19)NC_000011.9Chr1176,745,56176,745,561+
    nssv18792446Submitted genomicGRCh37 (hg19)NC_000011.9Chr1195,030,21495,030,214+
    nssv18792450Submitted genomicGRCh37 (hg19)NC_000011.9Chr1195,030,22195,030,221-

    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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