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nsv6718073

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,640

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 199 SVs from 47 studies. See in: genome view    
    Submitted genomic233,720,804-233,735,443Question Mark
    Overlapping variant regions from other studies: 199 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):234,629,450-234,644,089Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6718073Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2233,720,804233,735,443
    nsv6718073RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2234,629,450234,644,089

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450690deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450690Submitted genomicNC_000002.12:g.233
    720804_233735443de
    l
    GRCh38 (hg38)NC_000002.12Chr2233,720,804233,735,443
    nssv18450690RemappedPerfectNC_000002.11:g.234
    629450_234644089de
    l
    GRCh37.p13First PassNC_000002.11Chr2234,629,450234,644,089

    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)
    nssv184506901.4e-054275340
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