A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799918



Internal ID18825135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55615681..55647540hg38UCSC Ensembl
Innerchr11:55383157..55415016hg19UCSC Ensembl
Innerchr11:55139733..55171592hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3831860
hg1931860
hg1831860
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892007
Supporting Variants
Samples
Known GenesOR4P4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799918
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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