A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067191



Internal ID18809722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50023786..50135306hg38UCSC Ensembl
Innerchr19:50527043..50638563hg19UCSC Ensembl
Innerchr19:55218855..55330375hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38111521
hg19111521
hg18111521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574990
Samples
Known GenesFLJ26850, SNAR-A10, SNAR-A11, SNAR-A14, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-B1, SNAR-B2, VRK3, ZNF473
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067191
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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