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nsv6828570

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:512,440

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1349 SVs from 85 studies. See in: genome view    
    Submitted genomic134,250,795-134,763,234Question Mark
    Overlapping variant regions from other studies: 1349 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):133,935,547-134,447,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6828570Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7134,250,795134,763,234
    nsv6828570RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7133,935,547134,447,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18721035duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18721035Submitted genomicNC_000007.14:g.134
    250795_134763234du
    p
    GRCh38 (hg38)NC_000007.14Chr7134,250,795134,763,234
    nssv18721035RemappedPerfectNC_000007.13:g.133
    935547_134447985du
    p
    GRCh37.p13First PassNC_000007.13Chr7133,935,547134,447,985

    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)
    nssv187210354e-061274802
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