A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014996



Internal ID18757531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13278..84076hg38UCSC Ensembl
Innerchr4:13278..83967hg19UCSC Ensembl
Innerchr4:3278..73967hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3870799
hg1970690
hg1870690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5057n100
Supporting Variantsnssv3615231
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)nsv1014996
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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