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nsv6708505

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,982

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 22 studies. See in: genome view    
    Submitted genomic237,667,052-237,673,033Question Mark
    Overlapping variant regions from other studies: 198 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):238,575,695-238,581,676Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708505Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,667,052237,673,033
    nsv6708505RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,575,695238,581,676

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18462150deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18462150Submitted genomicNC_000002.12:g.237
    667052_237673033de
    l
    GRCh38 (hg38)NC_000002.12Chr2237,667,052237,673,033
    nssv18462150RemappedPerfectNC_000002.11:g.238
    575695_238581676de
    l
    GRCh37.p13First PassNC_000002.11Chr2238,575,695238,581,676

    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)
    nssv184621504e-061275852
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