A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796150



Internal ID18816699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162171774..162329393hg38UCSC Ensembl
Innerchr6:162592806..162750425hg19UCSC Ensembl
Innerchr6:162512796..162670415hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38157620
hg19157620
hg18157620
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890980
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796150
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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