A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639488



Internal ID7026268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86720504..86725689hg38UCSC Ensembl
Innerchr16:86720522..86725671hg38UCSC Ensembl
Outerchr16:86720486..86725707hg38UCSC Ensembl
chr16:86754110..86759295hg19UCSC Ensembl
Innerchr16:86754128..86759277hg19UCSC Ensembl
Outerchr16:86754092..86759313hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385186
hg195186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15553961, essv15553960, essv15553958, essv15553959
SamplesNA20874, HG03773, HG03908, HG03870
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639488
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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