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nsv7003751

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:191,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 709 SVs from 69 studies. See in: genome view    
    Submitted genomic32,126,701-32,318,400Question Mark
    Overlapping variant regions from other studies: 709 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):29,706,664-29,898,363Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003751Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1832,126,70132,318,400
    nsv7003751RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1829,706,66429,898,363

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18634753duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18634753Submitted genomicNC_000018.10:g.321
    26701_32318400dup
    GRCh38 (hg38)NC_000018.10Chr1832,126,70132,318,400
    nssv18634753RemappedPerfectNC_000018.9:g.2970
    6664_29898363dup
    GRCh37.p13First PassNC_000018.9Chr1829,706,66429,898,363

    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)
    nssv186347537e-062275902
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