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nsv6407127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,276

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 32 studies. See in: genome view    
    Submitted genomic141,480,504-141,482,779Question Mark
    Overlapping variant regions from other studies: 108 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):140,860,071-140,862,346Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6407127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,480,504141,482,779
    nsv6407127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,860,071140,862,346

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125802deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125802Submitted genomicNC_000005.10:g.141
    480504_141482779de
    l
    GRCh38 (hg38)NC_000005.10Chr5141,480,504141,482,779
    nssv18125802RemappedPerfectNC_000005.9:g.1408
    60071_140862346del
    GRCh37.p13First PassNC_000005.9Chr5140,860,071140,862,346

    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)
    nssv18125802<0.001732056
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