A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065444



Internal ID19154663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46078703..46209238hg38UCSC Ensembl
Innerchr17:44156069..44286604hg19UCSC Ensembl
Innerchr17:41511888..41642381hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38130536
hg19130536
hg18130494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3180n100
Supporting Variantsnssv3545166
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065444
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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