A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15501786



Internal ID3855821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68883193..68904837hg38UCSC Ensembl
Innerchr16:68883193..68904837hg38UCSC Ensembl
Outerchr16:68882693..68905337hg38UCSC Ensembl
chr16:68917096..68938740hg19UCSC Ensembl
Innerchr16:68917096..68938740hg19UCSC Ensembl
Outerchr16:68916596..68939240hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3821645
hg1921645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638917
Supporting Variants
SamplesHG03488
Known GenesTANGO6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15501786
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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