A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638910



Internal ID6679007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68752755..68761780hg38UCSC Ensembl
chr16:68786658..68795683hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389026
hg199026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501632
SamplesHG01893
Known GenesCDH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638910
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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