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nsv6656432

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:150,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2008 SVs from 94 studies. See in: genome view    
    Submitted genomic860,901-1,011,800Question Mark
    Overlapping variant regions from other studies: 2008 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):796,281-947,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6656432Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1860,9011,011,800
    nsv6656432RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1796,281947,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640588duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640588Submitted genomicNC_000001.11:g.860
    901_1011800dup
    GRCh38 (hg38)NC_000001.11Chr1860,9011,011,800
    nssv18640588RemappedPerfectNC_000001.10:g.796
    281_947180dup
    GRCh37.p13First PassNC_000001.10Chr1796,281947,180

    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)
    nssv18640588<0.00161256006
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