A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638885



Internal ID6678982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67374512..67377441hg38UCSC Ensembl
Innerchr16:67374512..67377441hg38UCSC Ensembl
Outerchr16:67374303..67377711hg38UCSC Ensembl
chr16:67408415..67411344hg19UCSC Ensembl
Innerchr16:67408415..67411344hg19UCSC Ensembl
Outerchr16:67408206..67411614hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501428
SamplesHG02922
Known GenesLRRC36
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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