A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636451



Internal ID18934732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189274456..189664435hg38UCSC Ensembl
Innerchr4:190195610..190585589hg19UCSC Ensembl
Innerchr4:190432604..190822583hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38389980
hg19389980
hg18389980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032433
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)nssv3636451
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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