A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638916



Internal ID7025701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68847574..68907820hg38UCSC Ensembl
chr16:68881477..68941723hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3860247
hg1960247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501785
SamplesHG03488
Known GenesTANGO6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638916
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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