A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639185



Internal ID7025968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78008451..78045266hg38UCSC Ensembl
Innerchr16:78008456..78045261hg38UCSC Ensembl
Outerchr16:78008446..78045271hg38UCSC Ensembl
chr16:78042348..78079163hg19UCSC Ensembl
Innerchr16:78042353..78079158hg19UCSC Ensembl
Outerchr16:78042343..78079168hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3836816
hg1936816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15528367
SamplesHG01710
Known GenesCLEC3A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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