A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5156n100



Internal ID22791243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23640405..23721785hg38UCSC Ensembl
chr4:23642028..23723408hg19UCSC Ensembl
chr4:23251126..23332506hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3881381
hg1981381
hg1881381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012746, nsv1008694, nsv1005174, nsv1009645, nsv1010544
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)dgv5156n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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