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nsv6711038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:166

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
    Submitted genomic119,538,075-119,538,240Question Mark
    Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):119,256,922-119,257,087Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3119,538,075119,538,240
    nsv6711038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3119,256,922119,257,087

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18670298duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18670298Submitted genomicNC_000003.12:g.119
    538075_119538240du
    p
    GRCh38 (hg38)NC_000003.12Chr3119,538,075119,538,240
    nssv18670298RemappedPerfectNC_000003.11:g.119
    256922_119257087du
    p
    GRCh37.p13First PassNC_000003.11Chr3119,256,922119,257,087

    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)
    nssv186702988e-062233954
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