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nsv6437047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,677

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 39 studies. See in: genome view    
    Submitted genomic121,934,743-121,980,419Question Mark
    Overlapping variant regions from other studies: 240 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):123,694,258-123,739,934Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6437047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10121,934,743121,980,419
    nsv6437047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10123,694,258123,739,934

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17978187deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17978187Submitted genomicNC_000010.11:g.121
    934743_121980419de
    l
    GRCh38 (hg38)NC_000010.11Chr10121,934,743121,980,419
    nssv17978187RemappedPerfectNC_000010.10:g.123
    694258_123739934de
    l
    GRCh37.p13First PassNC_000010.10Chr10123,694,258123,739,934

    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)
    nssv17978187<0.001139242
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