A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638860



Internal ID7025645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65818290..65829475hg38UCSC Ensembl
Innerchr16:65818293..65829472hg38UCSC Ensembl
Outerchr16:65818287..65829478hg38UCSC Ensembl
chr16:65852193..65863378hg19UCSC Ensembl
Innerchr16:65852196..65863375hg19UCSC Ensembl
Outerchr16:65852190..65863381hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811186
hg1911186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501075
SamplesHG01980
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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