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nsv6837736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:340,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1066 SVs from 84 studies. See in: genome view    
    Submitted genomic128,633,501-128,974,300Question Mark
    Overlapping variant regions from other studies: 1066 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):128,273,555-128,614,354Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6837736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,633,501128,974,300
    nsv6837736RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,273,555128,614,354

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723128duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723128Submitted genomicNC_000007.14:g.128
    633501_128974300du
    p
    GRCh38 (hg38)NC_000007.14Chr7128,633,501128,974,300
    nssv18723128RemappedPerfectNC_000007.13:g.128
    273555_128614354du
    p
    GRCh37.p13First PassNC_000007.13Chr7128,273,555128,614,354

    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)
    nssv187231288.8e-0523256650
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