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nsv6881535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167,931

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 502 SVs from 60 studies. See in: genome view    
    Submitted genomic97,075,720-97,243,650Question Mark
    Overlapping variant regions from other studies: 502 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):98,835,477-99,003,407Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6881535Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1097,075,72097,243,650
    nsv6881535RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1098,835,47799,003,407

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587343duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587343Submitted genomicNC_000010.11:g.970
    75720_97243650dup
    GRCh38 (hg38)NC_000010.11Chr1097,075,72097,243,650
    nssv18587343RemappedPerfectNC_000010.10:g.988
    35477_99003407dup
    GRCh37.p13First PassNC_000010.10Chr1098,835,47799,003,407

    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)
    nssv185873437e-062275510
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