A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9345n54



Internal ID22777240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160909586..161034677hg38UCSC Ensembl
chr4:161830738..161955829hg19UCSC Ensembl
chr4:162050188..162175279hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38125092
hg19125092
hg18125092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595879, nsv595882, nsv595876, nsv595877, nsv595881, nsv595880, nsv595878
SamplesHGDP01308, HGDP00955, HGDP01288, HGDP00774, HGDP00785, HGDP00762, HGDP01310
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9345n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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