A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15567786



Internal ID5569602
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639568
Supporting Variants
SamplesHG04134
Known GenesACSF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15567786
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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