A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619944



Internal ID7006817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20935733..20947222hg38UCSC Ensembl
chr9:20935732..20947221hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3811490
hg1911490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13416436
SamplesNA18643
Known GenesFOCAD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619944
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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