A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065648



Internal ID19154867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49924738..50001154hg38UCSC Ensembl
Innerchr19:50427995..50504411hg19UCSC Ensembl
Innerchr19:55119807..55196223hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3876417
hg1976417
hg1876417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724910
Samples
Known GenesATF5, IL4I1, MIR4751, NUP62, SIGLEC11, SIGLEC16, VRK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065648
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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