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nsv6601568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,091

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 35 studies. See in: genome view    
    Submitted genomic100,078,427-100,082,517Question Mark
    Overlapping variant regions from other studies: 120 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):99,676,050-99,680,140Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6601568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,078,427100,082,517
    nsv6601568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,676,05099,680,140

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18225252duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18225252Submitted genomicNC_000007.14:g.100
    078427_100082517du
    p
    GRCh38 (hg38)NC_000007.14Chr7100,078,427100,082,517
    nssv18225252RemappedPerfectNC_000007.13:g.996
    76050_99680140dup
    GRCh37.p13First PassNC_000007.13Chr799,676,05099,680,140

    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)
    nssv18225252<0.001139252
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