A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169755



Internal ID21313566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38950674..38955461hg38UCSC Ensembl
Outerchr22:38947911..38967614hg38UCSC Ensembl
Innerchr22:39346679..39351466hg19UCSC Ensembl
Outerchr22:39343916..39363619hg19UCSC Ensembl
Innerchr22:37676625..37681412hg18UCSC Ensembl
Outerchr22:37673862..37693565hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3819704
hg1919704
hg1819704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242585, nssv14240865
SamplesNGO_2, NGO_1
Known GenesAPOBEC3A, APOBEC3A_B
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169755
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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