A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892844



Internal ID19183664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32092598..32211736hg38UCSC Ensembl
Outerchr16:31990503..32211736hg38UCSC Ensembl
Innerchr16:32103919..32223057hg19UCSC Ensembl
Outerchr16:32001824..32223057hg19UCSC Ensembl
Innerchr16:32011420..32130558hg18UCSC Ensembl
Outerchr16:31909325..32130558hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38221234
hg19221234
hg18221234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792450, essv25791791
Samples
Known GenesHERC2P4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892844
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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