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nsv6343320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,644

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1115 SVs from 83 studies. See in: genome view    
    Submitted genomic241,462,667-241,628,310Question Mark
    Overlapping variant regions from other studies: 1115 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):242,402,082-242,567,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6343320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2241,462,667241,628,310
    nsv6343320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,402,082242,567,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18209013duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18209013Submitted genomicNC_000002.12:g.241
    462667_241628310du
    p
    GRCh38 (hg38)NC_000002.12Chr2241,462,667241,628,310
    nssv18209013RemappedPerfectNC_000002.11:g.242
    402082_242567725du
    p
    GRCh37.p13First PassNC_000002.11Chr2242,402,082242,567,725

    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)
    nssv18209013<0.001139296
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