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nsv6777781

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,142

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 23 studies. See in: genome view    
    Submitted genomic76,426,890-76,432,031Question Mark
    Overlapping variant regions from other studies: 108 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):75,722,715-75,727,856Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6777781Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr576,426,89076,432,031
    nsv6777781RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,722,71575,727,856

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516402deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516402Submitted genomicNC_000005.10:g.764
    26890_76432031del
    GRCh38 (hg38)NC_000005.10Chr576,426,89076,432,031
    nssv18516402RemappedPerfectNC_000005.9:g.7572
    2715_75727856del
    GRCh37.p13First PassNC_000005.9Chr575,722,71575,727,856

    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)
    nssv185164024e-061274742
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