A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787299



Internal ID19165124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8662843..8682560hg38UCSC Ensembl
Innerchr8:8520353..8540070hg19UCSC Ensembl
Innerchr8:8557763..8577480hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3819718
hg1919718
hg1819718
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891328
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787299
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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