A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4425n54



Internal ID18996601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30606930..30831032hg38UCSC Ensembl
chr15:30899133..31123235hg19UCSC Ensembl
chr15:28686425..28910527hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38224103
hg19224103
hg18224103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568751, nsv568761, nsv568759, nsv568754, nsv568753, nsv568750, nsv568760
SamplesHGDP01214
Known GenesARHGAP11B, GOLGA8H, HERC2P10, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4425n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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