A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639474



Internal ID7026254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86054333..86062121hg38UCSC Ensembl
Innerchr16:86054333..86062121hg38UCSC Ensembl
Outerchr16:86053833..86062621hg38UCSC Ensembl
chr16:86087939..86095727hg19UCSC Ensembl
Innerchr16:86087939..86095727hg19UCSC Ensembl
Outerchr16:86087439..86096227hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg387789
hg197789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15552549
SamplesNA18964
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639474
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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