A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15532536



Internal ID6614262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79967371..79995052hg38UCSC Ensembl
Innerchr16:79967387..79995036hg38UCSC Ensembl
Outerchr16:79967355..79995068hg38UCSC Ensembl
chr16:80001268..80028949hg19UCSC Ensembl
Innerchr16:80001284..80028933hg19UCSC Ensembl
Outerchr16:80001252..80028965hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3827682
hg1927682
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639257
Supporting Variants
SamplesNA20778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15532536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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