A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785807



Internal ID19173094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6972691..6991683hg38UCSC Ensembl
Innerchr11:6993922..7012914hg19UCSC Ensembl
Innerchr11:6950498..6969490hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3818993
hg1918993
hg1818993
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891924
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785807
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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