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nsv6815634

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 17 studies. See in: genome view    
    Submitted genomic111,500,893-111,500,938Question Mark
    Overlapping variant regions from other studies: 101 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):111,822,096-111,822,141Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6815634Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6111,500,893111,500,938
    nsv6815634RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6111,822,096111,822,141

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18520084deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18520084Submitted genomicNC_000006.12:g.111
    500893_111500938de
    l
    GRCh38 (hg38)NC_000006.12Chr6111,500,893111,500,938
    nssv18520084RemappedPerfectNC_000006.11:g.111
    822096_111822141de
    l
    GRCh37.p13First PassNC_000006.11Chr6111,822,096111,822,141

    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)
    nssv185200840.004860238274
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