A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635986



Internal ID18934267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29069658..29087787hg38UCSC Ensembl
Innerchr5:29069765..29087894hg19UCSC Ensembl
Innerchr5:29105522..29123651hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3818130
hg1918130
hg1818130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034864
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635986
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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