A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9351n54



Internal ID22777246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161006375..161082472hg38UCSC Ensembl
chr4:161927527..162003624hg19UCSC Ensembl
chr4:162146977..162223074hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3876098
hg1976098
hg1876098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595922, nsv595921, nsv595923, nsv595925, nsv595924, nsv595920, nsv595919
SamplesNINDS_155, HGDP00947, HGDP00527
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9351n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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