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nsv6951516

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:915,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3089 SVs from 91 studies. See in: genome view    
    Submitted genomic97,991,801-98,907,000Question Mark
    Overlapping variant regions from other studies: 3089 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):98,644,055-99,559,254Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6951516Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1397,991,80198,907,000
    nsv6951516RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1398,644,05599,559,254

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611610duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611610Submitted genomicNC_000013.11:g.979
    91801_98907000dup
    GRCh38 (hg38)NC_000013.11Chr1397,991,80198,907,000
    nssv18611610RemappedPerfectNC_000013.10:g.986
    44055_99559254dup
    GRCh37.p13First PassNC_000013.10Chr1398,644,05599,559,254

    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)
    nssv186116101.4e-054273590
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