A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv488n172



Internal ID22814862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38961235..38992489hg38UCSC Ensembl
chr22:39357240..39388494hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831255
hg1931255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4433441, nsv4433442, nsv4433440
SamplesSMI034, BTQ038, NB07
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv488n172
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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