A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781972



Internal ID19176252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36134028..36205009hg38UCSC Ensembl
Innerchr11:36155578..36226559hg19UCSC Ensembl
Innerchr11:36112154..36183135hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3870982
hg1970982
hg1870982
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891964
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781972
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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