nsv6871083

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 24 studies. See in: genome view    
    Submitted genomic35,679,183-35,681,319Question Mark
    Overlapping variant regions from other studies: 171 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):35,679,180-35,681,316Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6871083Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr935,679,18335,681,319
    nsv6871083RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr935,679,18035,681,316

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18567656deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18567656Submitted genomicNC_000009.12:g.356
    79183_35681319del
    GRCh38 (hg38)NC_000009.12Chr935,679,18335,681,319
    nssv18567656RemappedPerfectNC_000009.11:g.356
    79180_35681316del
    GRCh37.p13First PassNC_000009.11Chr935,679,18035,681,316

    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)
    nssv185676561.4e-054275766
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