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nsv6612957

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,143

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 36 studies. See in: genome view    
    Submitted genomic93,864,127-93,893,269Question Mark
    Overlapping variant regions from other studies: 151 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):93,493,439-93,522,581Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6612957Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr793,864,12793,893,269
    nsv6612957RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr793,493,43993,522,581

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18233706duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18233706Submitted genomicNC_000007.14:g.938
    64127_93893269dup
    GRCh38 (hg38)NC_000007.14Chr793,864,12793,893,269
    nssv18233706RemappedPerfectNC_000007.13:g.934
    93439_93522581dup
    GRCh37.p13First PassNC_000007.13Chr793,493,43993,522,581

    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)
    nssv18233706<0.001239260
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