A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796197



Internal ID19181883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533938..32551227hg38UCSC Ensembl
Innerchr6:32501715..32519004hg19UCSC Ensembl
Innerchr6:32609693..32626982hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3817290
hg1917290
hg1817290
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890834
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796197
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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