A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797267



Internal ID18835585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100436188..100519676hg38UCSC Ensembl
Innerchr8:101448416..101531904hg19UCSC Ensembl
Innerchr8:101517592..101601080hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3883489
hg1983489
hg1883489
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891450
Supporting Variants
Samples
Known GenesANKRD46
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797267
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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