A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787709



Internal ID19164963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16242771..16410993hg38UCSC Ensembl
Innerchr8:16100280..16268502hg19UCSC Ensembl
Innerchr8:16144651..16312873hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38168223
hg19168223
hg18168223
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891358
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787709
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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