A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780283



Internal ID19162095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21843050..21991057hg38UCSC Ensembl
Innerchr11:21864596..22012603hg19UCSC Ensembl
Innerchr11:21821172..21969179hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38148008
hg19148008
hg18148008
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=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780283
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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