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nsv6672276

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 24 studies. See in: genome view    
    Submitted genomic230,306,223-230,313,781Question Mark
    Overlapping variant regions from other studies: 147 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):230,441,969-230,449,527Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6672276Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1230,306,223230,313,781
    nsv6672276RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1230,441,969230,449,527

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370447deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370447Submitted genomicNC_000001.11:g.230
    306223_230313781de
    l
    GRCh38 (hg38)NC_000001.11Chr1230,306,223230,313,781
    nssv18370447RemappedPerfectNC_000001.10:g.230
    441969_230449527de
    l
    GRCh37.p13First PassNC_000001.10Chr1230,441,969230,449,527

    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)
    nssv183704473.5e-0510276244
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