A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797254



Internal ID19170843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80564619..80579673hg38UCSC Ensembl
Innerchr6:81274336..81289390hg19UCSC Ensembl
Innerchr6:81331055..81346109hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3815055
hg1915055
hg1815055
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890897
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797254
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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