A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647758



Internal ID7034497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39052369..39063994hg38UCSC Ensembl
Innerchr22:39052369..39063994hg38UCSC Ensembl
Outerchr22:39051869..39064494hg38UCSC Ensembl
chr22:39448374..39459999hg19UCSC Ensembl
Innerchr22:39448374..39459999hg19UCSC Ensembl
Outerchr22:39447874..39460499hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811626
hg1911626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16427697
SamplesNA19655
Known GenesAPOBEC3F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647758
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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