A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638156



Internal ID7024942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20763244..20764225hg38UCSC Ensembl
Innerchr16:20763294..20764175hg38UCSC Ensembl
Outerchr16:20763181..20764288hg38UCSC Ensembl
chr16:20774566..20775547hg19UCSC Ensembl
Innerchr16:20774616..20775497hg19UCSC Ensembl
Outerchr16:20774503..20775610hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38982
hg19982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15405030
SamplesHG01947
Known GenesACSM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638156
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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