A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792141



Internal ID18821414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149507931..149583818hg38UCSC Ensembl
Innerchr3:149225718..149301605hg19UCSC Ensembl
Innerchr3:150708408..150784295hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3875888
hg1975888
hg1875888
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893785
Supporting Variants
Samples
Known GenesWWTR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792141
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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