U.S. flag

An official website of the United States government

nsv6370753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:629

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 18 studies. See in: genome view    
    Submitted genomic154,336,268-154,336,896Question Mark
    Overlapping variant regions from other studies: 103 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):154,054,057-154,054,685Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6370753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,336,268154,336,896
    nsv6370753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,054,057154,054,685

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18096151deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18096151Submitted genomicNC_000003.12:g.154
    336268_154336896de
    l
    GRCh38 (hg38)NC_000003.12Chr3154,336,268154,336,896
    nssv18096151RemappedPerfectNC_000003.11:g.154
    054057_154054685de
    l
    GRCh37.p13First PassNC_000003.11Chr3154,054,057154,054,685

    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)
    nssv18096151<0.0011338362
    Support Center