A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796956



Internal ID19175416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121585151..121614456hg38UCSC Ensembl
Innerchr6:121906297..121935602hg19UCSC Ensembl
Innerchr6:121947996..121977301hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3829306
hg1929306
hg1829306
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890935
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796956
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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