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nsv6701142

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 287 SVs from 64 studies. See in: genome view    
    Submitted genomic98,114,001-98,174,700Question Mark
    Overlapping variant regions from other studies: 287 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):97,832,845-97,893,544Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6701142Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr398,114,00198,174,700
    nsv6701142RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr397,832,84597,893,544

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18488325deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18488325Submitted genomicNC_000003.12:g.981
    14001_98174700del
    GRCh38 (hg38)NC_000003.12Chr398,114,00198,174,700
    nssv18488325RemappedPerfectNC_000003.11:g.978
    32845_97893544del
    GRCh37.p13First PassNC_000003.11Chr397,832,84597,893,544

    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)
    nssv184883252.3e-056253678
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