A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891659



Internal ID19186055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:27939994..27982713hg38UCSC Ensembl
Outerchr2:27939994..27982713hg38UCSC Ensembl
Innerchr2:28162861..28205580hg19UCSC Ensembl
Outerchr2:28162861..28205580hg19UCSC Ensembl
Innerchr2:28016365..28059084hg18UCSC Ensembl
Outerchr2:28016365..28059084hg18UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3842720
hg1942720
hg1842720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797157
Samples
Known GenesBRE
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891659
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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