A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797252



Internal ID19169350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90799337..90855182hg38UCSC Ensembl
Innerchr11:90532505..90588350hg19UCSC Ensembl
Innerchr11:90172153..90227998hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3855846
hg1955846
hg1855846
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892061
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797252
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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