A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890935



Internal ID19185331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121585151..121614456hg38UCSC Ensembl
Outerchr6:121585151..121614456hg38UCSC Ensembl
Innerchr6:121906297..121935602hg19UCSC Ensembl
Outerchr6:121906297..121935602hg19UCSC Ensembl
Innerchr6:121947996..121977301hg18UCSC Ensembl
Outerchr6:121947996..121977301hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3829306
hg1929306
hg1829306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796956
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890935
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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