A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16425424



Internal ID6427240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38961689..38992569hg38UCSC Ensembl
Innerchr22:38962189..38992069hg38UCSC Ensembl
Outerchr22:38960689..38993569hg38UCSC Ensembl
chr22:39357694..39388574hg19UCSC Ensembl
Innerchr22:39358194..39388074hg19UCSC Ensembl
Outerchr22:39356694..39389574hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830881
hg1930881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647746
Supporting Variants
SamplesHG02113
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16425424
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer