A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4694n54



Internal ID20138118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85344022..85600273hg38UCSC Ensembl
chr15:85887253..86143504hg19UCSC Ensembl
chr15:83688257..83944508hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38256252
hg19256252
hg18256252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570309, nsv570313
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4694n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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