A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749490



Internal ID21385074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38961413..38991011hg38UCSC Ensembl
chr22:39357418..39387016hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3829599
hg1929599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433441
Supporting Variants
SamplesBTQ038
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749490
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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