A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016765



Internal ID18759300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:169202389..169328054hg38UCSC Ensembl
Innerchr5:168629393..168755058hg19UCSC Ensembl
Innerchr5:168561971..168687636hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38125666
hg19125666
hg18125666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649122
Samples
Known GenesMIR585, SLIT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016765
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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