A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555119



Internal ID3511592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87164512..87203913hg38UCSC Ensembl
Innerchr16:87164512..87203913hg38UCSC Ensembl
Outerchr16:87164334..87204196hg38UCSC Ensembl
chr16:87198118..87237519hg19UCSC Ensembl
Innerchr16:87198118..87237519hg19UCSC Ensembl
Outerchr16:87197940..87237802hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3839402
hg1939402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639504
Supporting Variants
SamplesHG03114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555119
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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