A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16427676



Internal ID6118686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39031590..39054994hg38UCSC Ensembl
chr22:39427595..39450999hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3823405
hg1923405
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647755
Supporting Variants
SamplesNA19655
Known GenesAPOBEC3D, APOBEC3F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16427676
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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