A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797157



Internal ID19181264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:27939994..27982713hg38UCSC Ensembl
Innerchr2:28162861..28205580hg19UCSC Ensembl
Innerchr2:28016365..28059084hg18UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3842720
hg1942720
hg1842720
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891659
Supporting Variants
Samples
Known GenesBRE
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797157
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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