A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638516



Internal ID18936797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2237476..2266191hg38UCSC Ensembl
Innerchr5:2237590..2266305hg19UCSC Ensembl
Innerchr5:2290590..2319305hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3828716
hg1928716
hg1828716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022951
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)nssv3638516
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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