A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796370



Internal ID19171866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101843467..102604238hg38UCSC Ensembl
Innerchr6:102291342..103052113hg19UCSC Ensembl
Innerchr6:102398035..103158806hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38760772
hg19760772
hg18760772
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890918
Supporting Variants
Samples
Known GenesGRIK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=117
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796370
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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