A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798036



Internal ID19180787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142025608..142055957hg38UCSC Ensembl
Innerchr6:142346745..142377094hg19UCSC Ensembl
Innerchr6:142388438..142418787hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3830350
hg1930350
hg1830350
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890956
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798036
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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