A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012094



Internal ID18754630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..159004hg38UCSC Ensembl
Innerchr4:12269..152794hg19UCSC Ensembl
Innerchr4:2269..142794hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38146736
hg19140526
hg18140526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5060n100
Supporting Variantsnssv3738051
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)nsv1012094
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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