A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9439n54



Internal ID20142863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186930134..188890842hg38UCSC Ensembl
chr4:187851288..189811996hg19UCSC Ensembl
chr4:188088282..190048990hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381960709
hg191960709
hg181960709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596446, nsv596443, nsv596447
Samples
Known GenesLINC01060, LOC339975, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9439n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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