A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695679



Internal ID15432331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:13531140..13542693hg38UCSC Ensembl
Innerchr5:13531250..13542802hg19UCSC Ensembl
Innerchr5:13584250..13595802hg18UCSC Ensembl
Innerchr5:13584250..13595802hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3811554
hg1911553
hg1811553
hg1711553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518248
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695679
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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