U.S. flag

An official website of the United States government

nsv6445025

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:403

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 191 SVs from 27 studies. See in: genome view    
    Submitted genomic133,518,523-133,518,925Question Mark
    Overlapping variant regions from other studies: 191 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):136,383,645-136,384,047Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6445025Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9133,518,523133,518,925
    nsv6445025RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9136,383,645136,384,047

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18177115deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18177115Submitted genomicNC_000009.12:g.133
    518523_133518925de
    l
    GRCh38 (hg38)NC_000009.12Chr9133,518,523133,518,925
    nssv18177115RemappedPerfectNC_000009.11:g.136
    383645_136384047de
    l
    GRCh37.p13First PassNC_000009.11Chr9136,383,645136,384,047

    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)
    nssv18177115<0.001233718
    Support Center