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nsv6400126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,063

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 29 studies. See in: genome view    
    Submitted genomic181,218,341-181,222,403Question Mark
    Overlapping variant regions from other studies: 149 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):180,645,341-180,649,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6400126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,218,341181,222,403
    nsv6400126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,645,341180,649,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18128356deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18128356Submitted genomicNC_000005.10:g.181
    218341_181222403de
    l
    GRCh38 (hg38)NC_000005.10Chr5181,218,341181,222,403
    nssv18128356RemappedPerfectNC_000005.9:g.1806
    45341_180649403del
    GRCh37.p13First PassNC_000005.9Chr5180,645,341180,649,403

    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)
    nssv18128356<0.001138522
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