U.S. flag

An official website of the United States government

nsv6357475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,028

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Submitted genomic157,540,075-157,546,102Question Mark
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):157,257,864-157,263,891Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6357475Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3157,540,075157,546,102
    nsv6357475RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3157,257,864157,263,891

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18096531deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18096531Submitted genomicNC_000003.12:g.157
    540075_157546102de
    l
    GRCh38 (hg38)NC_000003.12Chr3157,540,075157,546,102
    nssv18096531RemappedPerfectNC_000003.11:g.157
    257864_157263891de
    l
    GRCh37.p13First PassNC_000003.11Chr3157,257,864157,263,891

    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)
    nssv18096531<0.001139216
    Support Center