A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017141



Internal ID18759676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32615443..32722393hg38UCSC Ensembl
Innerchr5:32615549..32722499hg19UCSC Ensembl
Innerchr5:32651306..32758256hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38106951
hg19106951
hg18106951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3637049
Samples
Known GenesNPR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017141
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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