A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785199



Internal ID19170753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21843050..21989175hg38UCSC Ensembl
Innerchr11:21864596..22010721hg19UCSC Ensembl
Innerchr11:21821172..21967297hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38146126
hg19146126
hg18146126
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891946
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785199
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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