A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8623n54



Internal ID20142047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141876438..141877262hg38UCSC Ensembl
chr3:141595280..141596104hg19UCSC Ensembl
chr3:143077970..143078794hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38825
hg19825
hg18825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591903, nsv591904
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8623n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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