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nsv6977014

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 320 SVs from 44 studies. See in: genome view    
    Submitted genomic75,897,401-76,004,100Question Mark
    Overlapping variant regions from other studies: 320 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):76,363,744-76,470,443Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977014Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1475,897,40176,004,100
    nsv6977014RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1476,363,74476,470,443

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617952duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617952Submitted genomicNC_000014.9:g.7589
    7401_76004100dup
    GRCh38 (hg38)NC_000014.9Chr1475,897,40176,004,100
    nssv18617952RemappedPerfectNC_000014.8:g.7636
    3744_76470443dup
    GRCh37.p13First PassNC_000014.8Chr1476,363,74476,470,443

    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)
    nssv186179526.2e-0516254544
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