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nsv6383403

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
    Submitted genomic99,945,801-99,946,900Question Mark
    Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):100,866,958-100,868,057Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6383403Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr499,945,80199,946,900
    nsv6383403RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4100,866,958100,868,057

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18214424duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18214424Submitted genomicNC_000004.12:g.999
    45801_99946900dup
    GRCh38 (hg38)NC_000004.12Chr499,945,80199,946,900
    nssv18214424RemappedPerfectNC_000004.11:g.100
    866958_100868057du
    p
    GRCh37.p13First PassNC_000004.11Chr4100,866,958100,868,057

    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)
    nssv18214424<0.001135932
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