A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638147



Internal ID7024933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20541752..20557011hg38UCSC Ensembl
chr16:20553074..20568333hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3815260
hg1915260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15404965, essv15404964, essv15404963
SamplesHG01620, HG01108, HG01805
Known GenesACSM2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638147
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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