A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782652



Internal ID19164524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16611256..16719048hg38UCSC Ensembl
Innerchr8:16468765..16576557hg19UCSC Ensembl
Innerchr8:16513136..16620928hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38107793
hg19107793
hg18107793
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891361
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782652
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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