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nsv6896504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,197

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Submitted genomic1,030,227-1,034,423Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):1,076,167-1,080,363Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6896504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr101,030,2271,034,423
    nsv6896504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr101,076,1671,080,363

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18347503deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18347503Submitted genomicNC_000010.11:g.103
    0227_1034423del
    GRCh38 (hg38)NC_000010.11Chr101,030,2271,034,423
    nssv18347503RemappedPerfectNC_000010.10:g.107
    6167_1080363del
    GRCh37.p13First PassNC_000010.10Chr101,076,1671,080,363

    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)
    nssv183475034e-061275590
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