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nsv6943850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,629

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 35 studies. See in: genome view    
    Submitted genomic46,224,258-46,233,886Question Mark
    Overlapping variant regions from other studies: 154 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):46,798,393-46,808,021Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6943850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1346,224,25846,233,886
    nsv6943850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1346,798,39346,808,021

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378161deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378161Submitted genomicNC_000013.11:g.462
    24258_46233886del
    GRCh38 (hg38)NC_000013.11Chr1346,224,25846,233,886
    nssv18378161RemappedPerfectNC_000013.10:g.467
    98393_46808021del
    GRCh37.p13First PassNC_000013.10Chr1346,798,39346,808,021

    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)
    nssv183781614e-061276256
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