A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619959



Internal ID7006832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21251090..21278744hg38UCSC Ensembl
chr9:21251089..21278743hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3827655
hg1927655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13419256, essv13419259, essv13419258, essv13419257
SamplesHG01110, HG01047, NA19338, NA19747
Known GenesIFNA22P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619959
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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