A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647628



Internal ID6687682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33485609..33489492hg38UCSC Ensembl
Innerchr22:33485609..33489492hg38UCSC Ensembl
Outerchr22:33485541..33489648hg38UCSC Ensembl
chr22:33881595..33885478hg19UCSC Ensembl
Innerchr22:33881595..33885478hg19UCSC Ensembl
Outerchr22:33881527..33885634hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383884
hg193884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16408488
SamplesHG03867
Known GenesLARGE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647628
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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