A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797239



Internal ID18822258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78710128..78731403hg38UCSC Ensembl
Innerchr8:79622363..79643638hg19UCSC Ensembl
Innerchr8:79784918..79806193hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3821276
hg1921276
hg1821276
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891420
Supporting Variants
Samples
Known GenesLOC101241902, ZC2HC1A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797239
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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