A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9442n54



Internal ID22777337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187776941..188300053hg38UCSC Ensembl
chr4:188698095..189221207hg19UCSC Ensembl
chr4:188935089..189458201hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38523113
hg19523113
hg18523113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596454, nsv596455
SamplesHGDP01033
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9442n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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