A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787858



Internal ID19171936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104387864..104451150hg38UCSC Ensembl
Innerchr1:104930486..104993772hg19UCSC Ensembl
Innerchr1:104732009..104795295hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3863287
hg1963287
hg1863287
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893901
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787858
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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