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nsv6461104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,202

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 29 studies. See in: genome view    
    Submitted genomic62,209,635-62,237,836Question Mark
    Overlapping variant regions from other studies: 120 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):61,977,107-62,005,308Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6461104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1162,209,63562,237,836
    nsv6461104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1161,977,10762,005,308

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18196695duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18196695Submitted genomicNC_000011.10:g.622
    09635_62237836dup
    GRCh38 (hg38)NC_000011.10Chr1162,209,63562,237,836
    nssv18196695RemappedPerfectNC_000011.9:g.6197
    7107_62005308dup
    GRCh37.p13First PassNC_000011.9Chr1161,977,10762,005,308

    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)
    nssv18196695<0.0011339270
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