A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242585



Internal ID21303979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38950674..38967613hg38UCSC Ensembl
Outerchr22:38947911..38967614hg38UCSC Ensembl
Innerchr22:39346679..39363618hg19UCSC Ensembl
Outerchr22:39343916..39363619hg19UCSC Ensembl
Innerchr22:37676625..37693564hg18UCSC Ensembl
Outerchr22:37673862..37693565hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3819704
hg1919704
hg1819704
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169755
Supporting Variants
SamplesNGO_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)nssv14242585
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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