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nsv6705739

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 214 SVs from 49 studies. See in: genome view    
    Submitted genomic233,739,701-233,750,400Question Mark
    Overlapping variant regions from other studies: 214 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):234,648,347-234,659,046Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6705739Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2233,739,701233,750,400
    nsv6705739RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2234,648,347234,659,046

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450696deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450696Submitted genomicNC_000002.12:g.233
    739701_233750400de
    l
    GRCh38 (hg38)NC_000002.12Chr2233,739,701233,750,400
    nssv18450696RemappedPerfectNC_000002.11:g.234
    648347_234659046de
    l
    GRCh37.p13First PassNC_000002.11Chr2234,648,347234,659,046

    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)
    nssv18450696<0.00139254016
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