A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798045



Internal ID18820969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162203614..162485562hg38UCSC Ensembl
Innerchr6:162624646..162906594hg19UCSC Ensembl
Innerchr6:162544636..162826584hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38281949
hg19281949
hg18281949
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890984
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=85
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798045
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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