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nsv6642476

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,699

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 37 studies. See in: genome view    
    Submitted genomic154,313,448-154,342,146Question Mark
    Overlapping variant regions from other studies: 201 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):154,285,924-154,314,622Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642476Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1154,313,448154,342,146
    nsv6642476RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1154,285,924154,314,622

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587039duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587039Submitted genomicNC_000001.11:g.154
    313448_154342146du
    p
    GRCh38 (hg38)NC_000001.11Chr1154,313,448154,342,146
    nssv18587039RemappedPerfectNC_000001.10:g.154
    285924_154314622du
    p
    GRCh37.p13First PassNC_000001.10Chr1154,285,924154,314,622

    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)
    nssv185870394e-061275240
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