A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800282



Internal ID18815177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72054432..72074194hg38UCSC Ensembl
Innerchr16:72088331..72108093hg19UCSC Ensembl
Innerchr16:70645832..70665594hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3819763
hg1919763
hg1819763
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892884
Supporting Variants
Samples
Known GenesHP, HPR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800282
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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