A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788305



Internal ID19182277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70497685..70532127hg38UCSC Ensembl
Innerchr1:70963368..70997810hg19UCSC Ensembl
Innerchr1:70735956..70770398hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3834443
hg1934443
hg1834443
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893645
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788305
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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