A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006732



Internal ID22068363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22809019..23248080hg38UCSC Ensembl
Outerchr11:22808211..23250950hg38UCSC Ensembl
Innerchr11:22830565..23269626hg19UCSC Ensembl
Outerchr11:22829757..23272496hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38442740
hg19442740
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154704
Supporting Variants
Samples
Known GenesCCDC179, GAS2, SVIP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006732
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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