U.S. flag

An official website of the United States government

nsv6359411

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Submitted genomic87,123,201-87,127,400Question Mark
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):87,172,351-87,176,550Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6359411Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr387,123,20187,127,400
    nsv6359411RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr387,172,35187,176,550

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18104155deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18104155Submitted genomicNC_000003.12:g.871
    23201_87127400del
    GRCh38 (hg38)NC_000003.12Chr387,123,20187,127,400
    nssv18104155RemappedPerfectNC_000003.11:g.871
    72351_87176550del
    GRCh37.p13First PassNC_000003.11Chr387,172,35187,176,550

    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)
    nssv18104155<0.001139092
    Support Center