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nsv6993152

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,288

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 21 studies. See in: genome view    
    Submitted genomic58,783,903-58,791,190Question Mark
    Overlapping variant regions from other studies: 135 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):56,861,264-56,868,551Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993152Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,783,90358,791,190
    nsv6993152RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,861,26456,868,551

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413148deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413148Submitted genomicNC_000017.11:g.587
    83903_58791190del
    GRCh38 (hg38)NC_000017.11Chr1758,783,90358,791,190
    nssv18413148RemappedPerfectNC_000017.10:g.568
    61264_56868551del
    GRCh37.p13First PassNC_000017.10Chr1756,861,26456,868,551

    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)
    nssv184131487e-062276188
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