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nsv6451163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 18 studies. See in: genome view    
    Submitted genomic77,488,601-77,492,900Question Mark
    Overlapping variant regions from other studies: 95 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):80,103,517-80,107,816Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6451163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr977,488,60177,492,900
    nsv6451163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr980,103,51780,107,816

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18226956duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18226956Submitted genomicNC_000009.12:g.774
    88601_77492900dup
    GRCh38 (hg38)NC_000009.12Chr977,488,60177,492,900
    nssv18226956RemappedPerfectNC_000009.11:g.801
    03517_80107816dup
    GRCh37.p13First PassNC_000009.11Chr980,103,51780,107,816

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18226956<0.001639210
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