A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752708



Internal ID21388172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38961235..38991260hg38UCSC Ensembl
chr22:39357240..39387265hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830026
hg1930026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433440
Supporting Variants
SamplesNB07
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752708
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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