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nsv6977094

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,890

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Submitted genomic103,711,970-103,714,859Question Mark
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):104,178,307-104,181,196Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977094Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14103,711,970103,714,859
    nsv6977094RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14104,178,307104,181,196

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18383828deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18383828Submitted genomicNC_000014.9:g.1037
    11970_103714859del
    GRCh38 (hg38)NC_000014.9Chr14103,711,970103,714,859
    nssv18383828RemappedPerfectNC_000014.8:g.1041
    78307_104181196del
    GRCh37.p13First PassNC_000014.8Chr14104,178,307104,181,196

    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)
    nssv183838284e-061275636
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