A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638637



Internal ID7025422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52783191..52800707hg38UCSC Ensembl
chr16:52817103..52834619hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3817517
hg1917517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv520e214
Supporting Variantsessv15478695
SamplesNA20764
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638637
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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