A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6546187



Internal ID9741539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39030431..39050523hg38UCSC Ensembl
chr22:39426436..39446528hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3820093
hg1920093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676044
Supporting Variants
SamplesNA19678
Known GenesAPOBEC3D, APOBEC3F
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6546187
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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