A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790667



Internal ID19174288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82839762..83585301hg38UCSC Ensembl
Innerchr3:82888913..83634452hg19UCSC Ensembl
Innerchr3:82971603..83717142hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38745540
hg19745540
hg18745540
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893731
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=74
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790667
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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