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nsv6766228

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:454,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 993 SVs from 65 studies. See in: genome view    
    Submitted genomic34,948,101-35,402,800Question Mark
    Overlapping variant regions from other studies: 993 SVs from 65 studies. See in: genome view    
    Remapped(Score: Good):34,948,206-35,402,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6766228Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr534,948,10135,402,800
    nsv6766228RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr534,948,20635,402,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703278duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703278Submitted genomicNC_000005.10:g.349
    48101_35402800dup
    GRCh38 (hg38)NC_000005.10Chr534,948,10135,402,800
    nssv18703278RemappedGoodNC_000005.9:g.3494
    8206_35402902dup
    GRCh37.p13First PassNC_000005.9Chr534,948,20635,402,902

    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)
    nssv187032784e-0511271706
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