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nsv6935806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:307

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 32 studies. See in: genome view    
    Submitted genomic92,071,739-92,072,045Question Mark
    Overlapping variant regions from other studies: 111 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):92,465,515-92,465,821Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1292,071,73992,072,045
    nsv6935806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1292,465,51592,465,821

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18374325deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18374325Submitted genomicNC_000012.12:g.920
    71739_92072045del
    GRCh38 (hg38)NC_000012.12Chr1292,071,73992,072,045
    nssv18374325RemappedPerfectNC_000012.11:g.924
    65515_92465821del
    GRCh37.p13First PassNC_000012.11Chr1292,465,51592,465,821

    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)
    nssv183743250.0162699170238
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