A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785777



Internal ID18826168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55629099hg38UCSC Ensembl
Innerchr11:55373973..55396575hg19UCSC Ensembl
Innerchr11:55130549..55153151hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3822603
hg1922603
hg1822603
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892008
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785777
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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