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nsv6642960

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,687

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 31 studies. See in: genome view    
    Submitted genomic158,804,890-158,809,576Question Mark
    Overlapping variant regions from other studies: 138 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):158,774,680-158,779,366Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1158,804,890158,809,576
    nsv6642960RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1158,774,680158,779,366

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362549deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362549Submitted genomicNC_000001.11:g.158
    804890_158809576de
    l
    GRCh38 (hg38)NC_000001.11Chr1158,804,890158,809,576
    nssv18362549RemappedPerfectNC_000001.10:g.158
    774680_158779366de
    l
    GRCh37.p13First PassNC_000001.10Chr1158,774,680158,779,366

    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)
    nssv183625492.1e-056275032
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