A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786204



Internal ID18817315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70123665..70162409hg38UCSC Ensembl
Innerchr16:70157568..70196312hg19UCSC Ensembl
Innerchr16:68715069..68753813hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3838745
hg1938745
hg1838745
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892880
Supporting Variants
Samples
Known GenesPDPR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786204
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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