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nsv6323240

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,951

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 24 studies. See in: genome view    
    Submitted genomic19,973,897-19,975,847Question Mark
    Overlapping variant regions from other studies: 90 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):20,300,390-20,302,340Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6323240Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,973,89719,975,847
    nsv6323240RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr120,300,39020,302,340

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056562deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056562Submitted genomicNC_000001.11:g.199
    73897_19975847del
    GRCh38 (hg38)NC_000001.11Chr119,973,89719,975,847
    nssv18056562RemappedPerfectNC_000001.10:g.203
    00390_20302340del
    GRCh37.p13First PassNC_000001.10Chr120,300,39020,302,340

    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)
    nssv18056562<0.001138838
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