A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066058



Internal ID19155277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8917083..8977654hg38UCSC Ensembl
Innerchr19:9027759..9088330hg19UCSC Ensembl
Innerchr19:8888759..8949330hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3860572
hg1960572
hg1860572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564684
Samples
Known GenesMUC16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066058
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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