A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016966



Internal ID19106183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148288315..148419885hg38UCSC Ensembl
Innerchr4:149209467..149341037hg19UCSC Ensembl
Innerchr4:149428917..149560487hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38131571
hg19131571
hg18131571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636072
Samples
Known GenesNR3C2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016966
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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