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nsv6971902

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 33 studies. See in: genome view    
    Submitted genomic61,497,301-61,517,300Question Mark
    Overlapping variant regions from other studies: 164 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):61,964,019-61,984,018Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971902Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1461,497,30161,517,300
    nsv6971902RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1461,964,01961,984,018

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18387587deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18387587Submitted genomicNC_000014.9:g.6149
    7301_61517300del
    GRCh38 (hg38)NC_000014.9Chr1461,497,30161,517,300
    nssv18387587RemappedPerfectNC_000014.8:g.6196
    4019_61984018del
    GRCh37.p13First PassNC_000014.8Chr1461,964,01961,984,018

    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)
    nssv183875870.001283252452
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