A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433442



Internal ID21395444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38962355..38992489hg38UCSC Ensembl
chr22:39358360..39388494hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830135
hg1930135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv488n172
Supporting Variantsnssv15750983
SamplesSMI034
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433442
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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