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nsv7012921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101,306

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 469 SVs from 59 studies. See in: genome view    
    Submitted genomic58,325,544-58,426,849Question Mark
    Overlapping variant regions from other studies: 471 SVs from 59 studies. See in: genome view    
    Remapped(Score: Good):58,836,910-58,938,216Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,325,54458,426,849
    nsv7012921RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,836,91058,938,216

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640315duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640315Submitted genomicNC_000019.10:g.583
    25544_58426849dup
    GRCh38 (hg38)NC_000019.10Chr1958,325,54458,426,849
    nssv18640315RemappedGoodNC_000019.9:g.5883
    6910_58938216dup
    GRCh37.p13First PassNC_000019.9Chr1958,836,91058,938,216

    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)
    nssv186403151.4e-054273440
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