A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014869



Internal ID18757404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65773..209006hg38UCSC Ensembl
Innerchr4:65665..202795hg19UCSC Ensembl
Innerchr4:55665..192795hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38143234
hg19137131
hg18137131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5070n100
Supporting Variantsnssv3615289
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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