A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065753



Internal ID18808284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49974133..50067707hg38UCSC Ensembl
Innerchr19:50477390..50570964hg19UCSC Ensembl
Innerchr19:55169202..55262776hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3893575
hg1993575
hg1893575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574986
Samples
Known GenesFLJ26850, SIGLEC16, 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)nsv1065753
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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