A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639437



Internal ID7026218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84569011..84602293hg38UCSC Ensembl
Innerchr16:84569061..84602243hg38UCSC Ensembl
Outerchr16:84568961..84602343hg38UCSC Ensembl
chr16:84602617..84635899hg19UCSC Ensembl
Innerchr16:84602667..84635849hg19UCSC Ensembl
Outerchr16:84602567..84635949hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833283
hg1933283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv550e214
Supporting Variantsessv15547045
SamplesNA21127
Known GenesCOTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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