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nsv6813217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,747

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 22 studies. See in: genome view    
    Submitted genomic2,739,301-2,757,047Question Mark
    Overlapping variant regions from other studies: 151 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):2,778,935-2,796,681Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6813217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,739,3012,757,047
    nsv6813217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,778,9352,796,681

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18540155deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18540155Submitted genomicNC_000007.14:g.273
    9301_2757047del
    GRCh38 (hg38)NC_000007.14Chr72,739,3012,757,047
    nssv18540155RemappedPerfectNC_000007.13:g.277
    8935_2796681del
    GRCh37.p13First PassNC_000007.13Chr72,778,9352,796,681

    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)
    nssv185401557e-062276264
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