A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779472



Internal ID19172504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106860349..106881249hg38UCSC Ensembl
Innerchr8:107872577..107893477hg19UCSC Ensembl
Innerchr8:107941753..107962653hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3820901
hg1920901
hg1820901
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891456
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779472
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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