A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637675



Internal ID6677777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3851533..3861460hg38UCSC Ensembl
Innerchr16:3851562..3861431hg38UCSC Ensembl
Outerchr16:3851504..3861489hg38UCSC Ensembl
chr16:3901534..3911461hg19UCSC Ensembl
Innerchr16:3901563..3911432hg19UCSC Ensembl
Outerchr16:3901505..3911490hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389928
hg199928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363303
SamplesHG03196
Known GenesCREBBP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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