A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799420



Internal ID19171752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64548348..64672030hg38UCSC Ensembl
Innerchr16:64582251..64705933hg19UCSC Ensembl
Innerchr16:63139752..63263434hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38123683
hg19123683
hg18123683
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892874
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799420
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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