A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639072



Internal ID7025856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74582979..74594959hg38UCSC Ensembl
chr16:74616877..74628857hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3811981
hg1911981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv535e214
Supporting Variantsessv15518747
SamplesNA18530
Known GenesGLG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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