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nsv6638536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,992

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Submitted genomic101,914,941-101,917,932Question Mark
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):102,380,497-102,383,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6638536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,914,941101,917,932
    nsv6638536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,380,497102,383,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586345duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586345Submitted genomicNC_000001.11:g.101
    914941_101917932du
    p
    GRCh38 (hg38)NC_000001.11Chr1101,914,941101,917,932
    nssv18586345RemappedPerfectNC_000001.10:g.102
    380497_102383488du
    p
    GRCh37.p13First PassNC_000001.10Chr1102,380,497102,383,488

    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)
    nssv185863451.4e-054272502
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