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nsv6379848

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:460,264

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1238 SVs from 87 studies. See in: genome view    
    Submitted genomic118,193,140-118,653,403Question Mark
    Overlapping variant regions from other studies: 1238 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):119,114,295-119,574,558Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6379848Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4118,193,140118,653,403
    nsv6379848RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4119,114,295119,574,558

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211350duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211350Submitted genomicNC_000004.12:g.118
    193140_118653403du
    p
    GRCh38 (hg38)NC_000004.12Chr4118,193,140118,653,403
    nssv18211350RemappedPerfectNC_000004.11:g.119
    114295_119574558du
    p
    GRCh37.p13First PassNC_000004.11Chr4119,114,295119,574,558

    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)
    nssv18211350<0.001239220
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