A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639568



Internal ID6679659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89089424..89123537hg38UCSC Ensembl
Innerchr16:89089574..89123387hg38UCSC Ensembl
Outerchr16:89089274..89123687hg38UCSC Ensembl
chr16:89155832..89189945hg19UCSC Ensembl
Innerchr16:89155982..89189795hg19UCSC Ensembl
Outerchr16:89155682..89190095hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3834114
hg1934114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv554e214
Supporting Variantsessv15567786, essv15567787
SamplesNA18555, HG04134
Known GenesACSF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639568
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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