A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640761



Internal ID7027535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51308642..51329513hg38UCSC Ensembl
chr17:49386003..49406874hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3820872
hg1920872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15695685, essv15695683, essv15695684, essv15695682
SamplesHG01070, HG01058, HG01162, HG01191
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640761
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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