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nsv6692098

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:446

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Submitted genomic173,260,143-173,260,588Question Mark
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):174,124,871-174,125,316Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6692098Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2173,260,143173,260,588
    nsv6692098RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2174,124,871174,125,316

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18648603duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18648603Submitted genomicNC_000002.12:g.173
    260143_173260588du
    p
    GRCh38 (hg38)NC_000002.12Chr2173,260,143173,260,588
    nssv18648603RemappedPerfectNC_000002.11:g.174
    124871_174125316du
    p
    GRCh37.p13First PassNC_000002.11Chr2174,124,871174,125,316

    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)
    nssv18648603<0.00193222988
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