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nsv6407834

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:427

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 10 studies. See in: genome view    
    Submitted genomic149,093,561-149,093,987Question Mark
    Overlapping variant regions from other studies: 74 SVs from 10 studies. See in: genome view    
    Remapped(Score: Perfect):148,473,124-148,473,550Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6407834Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,093,561149,093,987
    nsv6407834RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5148,473,124148,473,550

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18126537deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18126537Submitted genomicNC_000005.10:g.149
    093561_149093987de
    l
    GRCh38 (hg38)NC_000005.10Chr5149,093,561149,093,987
    nssv18126537RemappedPerfectNC_000005.9:g.1484
    73124_148473550del
    GRCh37.p13First PassNC_000005.9Chr5148,473,124148,473,550

    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)
    nssv181265370.0014738846
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