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nsv6975374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,353

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
    Submitted genomic44,433,299-44,443,651Question Mark
    Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):44,725,497-44,735,849Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1544,433,29944,443,651
    nsv6975374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,725,49744,735,849

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18394707deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18394707Submitted genomicNC_000015.10:g.444
    33299_44443651del
    GRCh38 (hg38)NC_000015.10Chr1544,433,29944,443,651
    nssv18394707RemappedPerfectNC_000015.9:g.4472
    5497_44735849del
    GRCh37.p13First PassNC_000015.9Chr1544,725,49744,735,849

    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)
    nssv183947074e-060276266
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