A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781552



Internal ID18830202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3220993..3381247hg38UCSC Ensembl
Innerchr11:3242223..3402477hg19UCSC Ensembl
Innerchr11:3198799..3359053hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38160255
hg19160255
hg18160255
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891908
Supporting Variants
Samples
Known GenesLOC650368, MRGPRE, MRGPRG-AS1, ZNF195
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=43
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781552
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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