A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638242



Internal ID6678340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24078116..24079565hg38UCSC Ensembl
Innerchr16:24078128..24079553hg38UCSC Ensembl
Outerchr16:24078104..24079577hg38UCSC Ensembl
chr16:24089437..24090886hg19UCSC Ensembl
Innerchr16:24089449..24090874hg19UCSC Ensembl
Outerchr16:24089425..24090898hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15429928
SamplesHG04235
Known GenesPRKCB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638242
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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