A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787756



Internal ID19176680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23695630..23720880hg38UCSC Ensembl
Innerchr3:23737121..23762371hg19UCSC Ensembl
Innerchr3:23712125..23737375hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3825251
hg1925251
hg1825251
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893673
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787756
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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