A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065734



Internal ID18808265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47610045..47631849hg38UCSC Ensembl
Innerchr22:48005794..48027598hg19UCSC Ensembl
Innerchr22:46384458..46406262hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3821805
hg1921805
hg1821805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592275
Samples
Known GenesLINC00898
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065734
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer