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nsv6735265

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 54 studies. See in: genome view    
    Submitted genomic53,207,201-53,225,300Question Mark
    Overlapping variant regions from other studies: 176 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):54,073,368-54,091,467Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6735265Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr453,207,20153,225,300
    nsv6735265RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr454,073,36854,091,467

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18499824deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18499824Submitted genomicNC_000004.12:g.532
    07201_53225300del
    GRCh38 (hg38)NC_000004.12Chr453,207,20153,225,300
    nssv18499824RemappedPerfectNC_000004.11:g.540
    73368_54091467del
    GRCh37.p13First PassNC_000004.11Chr454,073,36854,091,467

    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)
    nssv184998243.9e-0511275782
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