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nsv6719128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:216,521

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 623 SVs from 58 studies. See in: genome view    
    Submitted genomic24,402,314-24,618,834Question Mark
    Overlapping variant regions from other studies: 623 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):24,403,937-24,620,457Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6719128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr424,402,31424,618,834
    nsv6719128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr424,403,93724,620,457

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18689248duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18689248Submitted genomicNC_000004.12:g.244
    02314_24618834dup
    GRCh38 (hg38)NC_000004.12Chr424,402,31424,618,834
    nssv18689248RemappedPerfectNC_000004.11:g.244
    03937_24620457dup
    GRCh37.p13First PassNC_000004.11Chr424,403,93724,620,457

    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)
    nssv186892487e-062274922
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