A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786699



Internal ID18821013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70107584..70157430hg38UCSC Ensembl
Innerchr16:70141487..70191333hg19UCSC Ensembl
Innerchr16:68698988..68748834hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3849847
hg1949847
hg1849847
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)essv25786699
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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