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nsv7056620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:359,165

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1078 SVs from 87 studies. See in: genome view    
    Submitted genomic233,572,655-233,931,819Question Mark
    Overlapping variant regions from other studies: 1078 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):234,481,301-234,840,464Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2233,572,655233,931,819
    nsv7056620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2234,481,301234,840,464

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767753inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767753Submitted genomicNC_000002.12:g.233
    572655_233931819in
    v
    GRCh38 (hg38)NC_000002.12Chr2233,572,655233,931,819
    nssv18767753RemappedPerfectNC_000002.11:g.234
    481301_234840464in
    v
    GRCh37.p13First PassNC_000002.11Chr2234,481,301234,840,464

    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)
    nssv187677534e-061276268
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