A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363800



Internal ID5665725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4735863..4738408hg38UCSC Ensembl
Innerchr16:4735863..4738408hg38UCSC Ensembl
Outerchr16:4735600..4738654hg38UCSC Ensembl
chr16:4785864..4788409hg19UCSC Ensembl
Innerchr16:4785864..4788409hg19UCSC Ensembl
Outerchr16:4785601..4788655hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637702
Supporting Variants
SamplesNA19075
Known GenesC16orf71
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363800
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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