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nsv7083819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:788,234

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1273 SVs from 69 studies. See in: genome view    
    Submitted genomic131,629,094-132,417,327Question Mark
    Overlapping variant regions from other studies: 1276 SVs from 69 studies. See in: genome view    
    Remapped(Score: Good):130,763,096-131,551,355Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX131,629,094132,417,327
    nsv7083819RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX130,763,096131,551,355

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653637duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653637Submitted genomicNC_000023.11:g.131
    629094_132417327du
    p
    GRCh38 (hg38)NC_000023.11ChrX131,629,094132,417,327
    nssv18653637RemappedGoodNC_000023.10:g.130
    763096_131551355du
    p
    GRCh37.p13First PassNC_000023.10ChrX130,763,096131,551,355

    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)
    nssv186536375e-061200000
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