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nsv7098701

  • 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: 188 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):113,327,375-113,327,375Question Mark
    Overlapping variant regions from other studies: 188 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):113,327,377-113,327,377Question Mark
    Overlapping variant regions from other studies: 170 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):113,518,619-113,518,619Question Mark
    Overlapping variant regions from other studies: 170 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):113,518,620-113,518,620Question Mark
    Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):113,788,286-113,788,286Question Mark
    Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):113,788,286-113,788,286Question Mark
    Overlapping variant regions from other studies: 180 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):113,914,806-113,914,806Question Mark
    Overlapping variant regions from other studies: 180 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):113,914,807-113,914,807Question Mark
    Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):114,094,222-114,094,222Question Mark
    Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):114,094,222-114,094,222Question Mark
    Overlapping variant regions from other studies: 186 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):121,597,201-121,597,201Question Mark
    Overlapping variant regions from other studies: 186 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):121,597,201-121,597,201Question Mark
    Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):78,799,545-78,799,545Question Mark
    Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):78,799,545-78,799,545Question Mark
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):81,854,080-81,854,080Question Mark
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):81,854,080-81,854,080Question Mark
    Overlapping variant regions from other studies: 68 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):14,301,475-14,301,475Question Mark
    Overlapping variant regions from other studies: 68 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):14,301,476-14,301,476Question Mark
    Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):16,399,832-16,399,832Question Mark
    Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):16,399,833-16,399,833Question Mark
    Overlapping variant regions from other studies: 188 SVs from 20 studies. See in: genome view    
    Submitted genomic114,339,604-114,339,604Question Mark
    Overlapping variant regions from other studies: 188 SVs from 20 studies. See in: genome view    
    Submitted genomic114,339,606-114,339,606Question Mark
    Overlapping variant regions from other studies: 170 SVs from 16 studies. See in: genome view    
    Submitted genomic114,530,848-114,530,848Question Mark
    Overlapping variant regions from other studies: 170 SVs from 16 studies. See in: genome view    
    Submitted genomic114,530,849-114,530,849Question Mark
    Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
    Submitted genomic114,800,515-114,800,515Question Mark
    Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
    Submitted genomic114,800,515-114,800,515Question Mark
    Overlapping variant regions from other studies: 180 SVs from 24 studies. See in: genome view    
    Submitted genomic114,927,035-114,927,035Question Mark
    Overlapping variant regions from other studies: 180 SVs from 24 studies. See in: genome view    
    Submitted genomic114,927,036-114,927,036Question Mark
    Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
    Submitted genomic115,106,451-115,106,451Question Mark
    Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
    Submitted genomic115,106,451-115,106,451Question Mark
    Overlapping variant regions from other studies: 186 SVs from 15 studies. See in: genome view    
    Submitted genomic122,609,441-122,609,441Question Mark
    Overlapping variant regions from other studies: 186 SVs from 15 studies. See in: genome view    
    Submitted genomic122,609,441-122,609,441Question Mark
    Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
    Submitted genomic79,711,780-79,711,780Question Mark
    Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
    Submitted genomic79,711,780-79,711,780Question Mark
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Submitted genomic82,766,315-82,766,315Question Mark
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Submitted genomic82,766,315-82,766,315Question Mark
    Overlapping variant regions from other studies: 68 SVs from 12 studies. See in: genome view    
    Submitted genomic14,343,474-14,343,474Question Mark
    Overlapping variant regions from other studies: 68 SVs from 12 studies. See in: genome view    
    Submitted genomic14,343,475-14,343,475Question Mark
    Overlapping variant regions from other studies: 149 SVs from 28 studies. See in: genome view    
    Submitted genomic16,552,766-16,552,766Question Mark
    Overlapping variant regions from other studies: 149 SVs from 28 studies. See in: genome view    
    Submitted genomic16,552,767-16,552,767Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,327,375113,327,375+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,327,377113,327,377-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,518,619113,518,619+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,518,620113,518,620-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,788,286113,788,286+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,788,286113,788,286-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,914,806113,914,806-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,914,807113,914,807+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,094,222114,094,222+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,094,222114,094,222-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8121,597,201121,597,201+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8121,597,201121,597,201-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr878,799,54578,799,545+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr878,799,54578,799,545-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr881,854,08081,854,080+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr881,854,08081,854,080-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1014,301,47514,301,475-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1014,301,47614,301,476+
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1216,399,83216,399,832-
    nsv7098701RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1216,399,83316,399,833+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,339,604114,339,604+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,339,606114,339,606-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,530,848114,530,848+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,530,849114,530,849-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,800,515114,800,515+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,800,515114,800,515-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,927,035114,927,035-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,927,036114,927,036+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,106,451115,106,451+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,106,451115,106,451-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8122,609,441122,609,441+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8122,609,441122,609,441-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr879,711,78079,711,780+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr879,711,78079,711,780-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr882,766,31582,766,315+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr882,766,31582,766,315-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1014,343,47414,343,474-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1014,343,47514,343,475+
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1216,552,76616,552,766-
    nsv7098701Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1216,552,76716,552,767+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792383intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792395intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792394interchromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792397interchromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792396intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792399intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792400intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792382intrachromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792398interchromosomal translocationFHU14-134SequencingSequence alignment10
    nssv18792381interchromosomal translocationFHU14-134SequencingSequence alignment10

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792383RemappedPerfectGRCh38.p12First PassNC_000008.11Chr878,799,54578,799,545+
    nssv18792395RemappedPerfectGRCh38.p12First PassNC_000008.11Chr878,799,54578,799,545-
    nssv18792394RemappedPerfectGRCh38.p12First PassNC_000008.11Chr881,854,08081,854,080+
    nssv18792397RemappedPerfectGRCh38.p12First PassNC_000008.11Chr881,854,08081,854,080-
    nssv18792396RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,327,375113,327,375+
    nssv18792399RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,327,377113,327,377-
    nssv18792400RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,518,619113,518,619+
    nssv18792395RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,518,620113,518,620-
    nssv18792396RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,788,286113,788,286+
    nssv18792399RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,788,286113,788,286-
    nssv18792382RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,914,806113,914,806-
    nssv18792398RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,914,807113,914,807+
    nssv18792383RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,094,222114,094,222+
    nssv18792400RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,094,222114,094,222-
    nssv18792381RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8121,597,201121,597,201+
    nssv18792382RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8121,597,201121,597,201-
    nssv18792398RemappedPerfectGRCh38.p12First PassNC_000010.11Chr1014,301,47514,301,475-
    nssv18792381RemappedPerfectGRCh38.p12First PassNC_000010.11Chr1014,301,47614,301,476+
    nssv18792394RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1216,399,83216,399,832-
    nssv18792397RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1216,399,83316,399,833+
    nssv18792383Submitted genomicGRCh37 (hg19)NC_000008.10Chr879,711,78079,711,780+
    nssv18792395Submitted genomicGRCh37 (hg19)NC_000008.10Chr879,711,78079,711,780-
    nssv18792394Submitted genomicGRCh37 (hg19)NC_000008.10Chr882,766,31582,766,315+
    nssv18792397Submitted genomicGRCh37 (hg19)NC_000008.10Chr882,766,31582,766,315-
    nssv18792396Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,339,604114,339,604+
    nssv18792399Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,339,606114,339,606-
    nssv18792400Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,530,848114,530,848+
    nssv18792395Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,530,849114,530,849-
    nssv18792396Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,800,515114,800,515+
    nssv18792399Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,800,515114,800,515-
    nssv18792382Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,927,035114,927,035-
    nssv18792398Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,927,036114,927,036+
    nssv18792383Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,106,451115,106,451+
    nssv18792400Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,106,451115,106,451-
    nssv18792381Submitted genomicGRCh37 (hg19)NC_000008.10Chr8122,609,441122,609,441+
    nssv18792382Submitted genomicGRCh37 (hg19)NC_000008.10Chr8122,609,441122,609,441-
    nssv18792398Submitted genomicGRCh37 (hg19)NC_000010.10Chr1014,343,47414,343,474-
    nssv18792381Submitted genomicGRCh37 (hg19)NC_000010.10Chr1014,343,47514,343,475+
    nssv18792394Submitted genomicGRCh37 (hg19)NC_000012.11Chr1216,552,76616,552,766-
    nssv18792397Submitted genomicGRCh37 (hg19)NC_000012.11Chr1216,552,76716,552,767+

    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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