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nsv6562725

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:570,653

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1276 SVs from 80 studies. See in: genome view    
    Submitted genomic161,386,305-161,956,957Question Mark
    Overlapping variant regions from other studies: 1276 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):161,104,093-161,674,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6562725Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3161,386,305161,956,957
    nsv6562725RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3161,104,093161,674,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18261067inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18261067Submitted genomicNC_000003.12:g.161
    386305_161956957in
    v
    GRCh38 (hg38)NC_000003.12Chr3161,386,305161,956,957
    nssv18261067RemappedPerfectNC_000003.11:g.161
    104093_161674745in
    v
    GRCh37.p13First PassNC_000003.11Chr3161,104,093161,674,745

    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)
    nssv18261067<0.001239304
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