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nsv6642974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:898,710

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1721 SVs from 89 studies. See in: genome view    
    Submitted genomic159,156,578-160,055,287Question Mark
    Overlapping variant regions from other studies: 1725 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):159,126,368-160,025,077Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642974Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1159,156,578160,055,287
    nsv6642974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1159,126,368160,025,077

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18574472duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18574472Submitted genomicNC_000001.11:g.159
    156578_160055287du
    p
    GRCh38 (hg38)NC_000001.11Chr1159,156,578160,055,287
    nssv18574472RemappedPerfectNC_000001.10:g.159
    126368_160025077du
    p
    GRCh37.p13First PassNC_000001.10Chr1159,126,368160,025,077

    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)
    nssv185744724e-061271690
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