A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639438



Internal ID7026219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84569436..84600799hg38UCSC Ensembl
chr16:84603042..84634405hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3831364
hg1931364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv550e214
Supporting Variantsessv15547046, essv15547048, essv15547047
SamplesNA21127, NA19467, NA19438
Known GenesCOTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639438
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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