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nsv6670950

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
    Submitted genomic63,884,795-63,887,291Question Mark
    Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):64,111,929-64,114,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6670950Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr263,884,79563,887,291
    nsv6670950RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr264,111,92964,114,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18468171deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18468171Submitted genomicNC_000002.12:g.638
    84795_63887291del
    GRCh38 (hg38)NC_000002.12Chr263,884,79563,887,291
    nssv18468171RemappedPerfectNC_000002.11:g.641
    11929_64114425del
    GRCh37.p13First PassNC_000002.11Chr264,111,92964,114,425

    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)
    nssv184681714e-061274402
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