A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639333



Internal ID7026116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81418252..81427666hg38UCSC Ensembl
Innerchr16:81418402..81427516hg38UCSC Ensembl
Outerchr16:81418102..81427816hg38UCSC Ensembl
chr16:81451857..81461271hg19UCSC Ensembl
Innerchr16:81452007..81461121hg19UCSC Ensembl
Outerchr16:81451707..81461421hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg389415
hg199415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537857, essv15537858, essv15537856
SamplesHG02661, HG02554, HG00258
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639333
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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