A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787984



Internal ID18822291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37265836..37589124hg38UCSC Ensembl
Innerchr13:37839973..38163261hg19UCSC Ensembl
Innerchr13:36737973..37061261hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38323289
hg19323289
hg18323289
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892331
Supporting Variants
Samples
Known GenesLINC00547, POSTN
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=92
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787984
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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