A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892884



Internal ID18837018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72054432..72074194hg38UCSC Ensembl
Outerchr16:72054432..72074194hg38UCSC Ensembl
Innerchr16:72088331..72108093hg19UCSC Ensembl
Outerchr16:72088331..72108093hg19UCSC Ensembl
Innerchr16:70645832..70665594hg18UCSC Ensembl
Outerchr16:70645832..70665594hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3819763
hg1919763
hg1819763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800282, essv25778587, essv25778637, essv25794869
Samples
Known GenesHP, HPR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892884
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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