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nsv6685285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 251 SVs from 31 studies. See in: genome view    
    Submitted genomic175,156,001-175,206,700Question Mark
    Overlapping variant regions from other studies: 251 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):176,020,729-176,071,428Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6685285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2175,156,001175,206,700
    nsv6685285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2176,020,729176,071,428

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18660835duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18660835Submitted genomicNC_000002.12:g.175
    156001_175206700du
    p
    GRCh38 (hg38)NC_000002.12Chr2175,156,001175,206,700
    nssv18660835RemappedPerfectNC_000002.11:g.176
    020729_176071428du
    p
    GRCh37.p13First PassNC_000002.11Chr2176,020,729176,071,428

    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)
    nssv18660835<0.001130267612
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