A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5162n100



Internal ID22791249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28271622..28641320hg38UCSC Ensembl
chr4:28273244..28642942hg19UCSC Ensembl
chr4:27882342..28252040hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38369699
hg19369699
hg18369699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014938, nsv1010133
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)dgv5162n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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