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nsv6971540

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,350

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 29 studies. See in: genome view    
    Submitted genomic92,556,233-92,559,582Question Mark
    Overlapping variant regions from other studies: 91 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):93,022,578-93,025,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971540Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1492,556,23392,559,582
    nsv6971540RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1493,022,57893,025,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391599deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391599Submitted genomicNC_000014.9:g.9255
    6233_92559582del
    GRCh38 (hg38)NC_000014.9Chr1492,556,23392,559,582
    nssv18391599RemappedPerfectNC_000014.8:g.9302
    2578_93025927del
    GRCh37.p13First PassNC_000014.8Chr1493,022,57893,025,927

    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)
    nssv183915993.2e-059275994
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