A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890918



Internal ID19185314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101843467..102604238hg38UCSC Ensembl
Outerchr6:101843467..102604238hg38UCSC Ensembl
Innerchr6:102291342..103052113hg19UCSC Ensembl
Outerchr6:102291342..103052113hg19UCSC Ensembl
Innerchr6:102398035..103158806hg18UCSC Ensembl
Outerchr6:102398035..103158806hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38760772
hg19760772
hg18760772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796370
Samples
Known GenesGRIK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890918
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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