A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786896



Internal ID18823854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85977166..85992931hg38UCSC Ensembl
Innerchr11:85688209..85703974hg19UCSC Ensembl
Innerchr11:85365857..85381622hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3815766
hg1915766
hg1815766
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892049
Supporting Variants
Samples
Known GenesPICALM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786896
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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