A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638866



Internal ID7025651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66025060..66037196hg38UCSC Ensembl
Innerchr16:66025210..66037046hg38UCSC Ensembl
Outerchr16:66024910..66037346hg38UCSC Ensembl
chr16:66058963..66071099hg19UCSC Ensembl
Innerchr16:66059113..66070949hg19UCSC Ensembl
Outerchr16:66058813..66071249hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3812137
hg1912137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501218
SamplesHG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638866
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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