A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569959



Internal ID5571775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89974426..89976186hg38UCSC Ensembl
Innerchr16:89974436..89976176hg38UCSC Ensembl
Outerchr16:89974416..89976196hg38UCSC Ensembl
chr16:90040834..90042594hg19UCSC Ensembl
Innerchr16:90040844..90042584hg19UCSC Ensembl
Outerchr16:90040824..90042604hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639604
Supporting Variants
SamplesHG03028
Known GenesAFG3L1P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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