A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797180



Internal ID19181660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41557765..41658633hg38UCSC Ensembl
Innerchr2:41784905..41885773hg19UCSC Ensembl
Innerchr2:41638409..41739277hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38100869
hg19100869
hg18100869
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891971
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797180
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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