A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16427697



Internal ID6118670
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647758
Supporting Variants
SamplesNA19655
Known GenesAPOBEC3F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16427697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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