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nsv6771692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,267

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
    Submitted genomic76,416,474-76,420,740Question Mark
    Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):75,712,299-75,716,565Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6771692Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr576,416,47476,420,740
    nsv6771692RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,712,29975,716,565

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516400deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516400Submitted genomicNC_000005.10:g.764
    16474_76420740del
    GRCh38 (hg38)NC_000005.10Chr576,416,47476,420,740
    nssv18516400RemappedPerfectNC_000005.9:g.7571
    2299_75716565del
    GRCh37.p13First PassNC_000005.9Chr575,712,29975,716,565

    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)
    nssv185164007e-062274476
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