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nsv6857285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,712

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 21 studies. See in: genome view    
    Submitted genomic76,783,175-76,786,886Question Mark
    Overlapping variant regions from other studies: 127 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):77,695,411-77,699,122Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr876,783,17576,786,886
    nsv6857285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr877,695,41177,699,122

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18558646deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18558646Submitted genomicNC_000008.11:g.767
    83175_76786886del
    GRCh38 (hg38)NC_000008.11Chr876,783,17576,786,886
    nssv18558646RemappedPerfectNC_000008.10:g.776
    95411_77699122del
    GRCh37.p13First PassNC_000008.10Chr877,695,41177,699,122

    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)
    nssv185586464e-061275480
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