A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638154



Internal ID7024940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20703114..20714638hg38UCSC Ensembl
Innerchr16:20703131..20714621hg38UCSC Ensembl
Outerchr16:20703097..20714655hg38UCSC Ensembl
chr16:20714436..20725960hg19UCSC Ensembl
Innerchr16:20714453..20725943hg19UCSC Ensembl
Outerchr16:20714419..20725977hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3811525
hg1911525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15405027
SamplesHG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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