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nsv6671536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:436,969

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1135 SVs from 74 studies. See in: genome view    
    Submitted genomic233,488,326-233,925,294Question Mark
    Overlapping variant regions from other studies: 1138 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):233,624,072-234,061,040Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6671536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1233,488,326233,925,294
    nsv6671536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1233,624,072234,061,040

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370275deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370275Submitted genomicNC_000001.11:g.233
    488326_233925294de
    l
    GRCh38 (hg38)NC_000001.11Chr1233,488,326233,925,294
    nssv18370275RemappedPerfectNC_000001.10:g.233
    624072_234061040de
    l
    GRCh37.p13First PassNC_000001.10Chr1233,624,072234,061,040

    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)
    nssv183702754e-061276160
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