A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011630



Internal ID19100847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:198052748..198107265hg38UCSC Ensembl
Innerchr3:197779619..197834136hg19UCSC Ensembl
Innerchr3:199264016..199318533hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3854518
hg1954518
hg1854518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5047n100
Supporting Variantsnssv3617039
Samples
Known GenesANKRD18DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011630
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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