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nsv6661083

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,427

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 23 studies. See in: genome view    
    Submitted genomic233,635,176-233,645,602Question Mark
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):233,770,922-233,781,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6661083Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1233,635,176233,645,602
    nsv6661083RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1233,770,922233,781,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370290deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370290Submitted genomicNC_000001.11:g.233
    635176_233645602de
    l
    GRCh38 (hg38)NC_000001.11Chr1233,635,176233,645,602
    nssv18370290RemappedPerfectNC_000001.10:g.233
    770922_233781348de
    l
    GRCh37.p13First PassNC_000001.10Chr1233,770,922233,781,348

    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)
    nssv183702904e-061276268
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