A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9311n54



Internal ID22777206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148444722..148445829hg38UCSC Ensembl
chr4:149365874..149366981hg19UCSC Ensembl
chr4:149585324..149586431hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381108
hg191108
hg181108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595681, nsv595682, nsv595680, nsv595683, nsv595684
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9311n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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