A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059224



Internal ID19148443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18899376..18918093hg38UCSC Ensembl
Innerchr22:18886889..18905606hg19UCSC Ensembl
Innerchr22:17266889..17285606hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3818718
hg1918718
hg1818718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4475n100
Supporting Variantsnssv3587292
Samples
Known GenesDGCR6, PRODH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059224
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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