A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014368



Internal ID19103587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3939505..4205592hg38UCSC Ensembl
Innerchr4:3941232..4207319hg19UCSC Ensembl
Innerchr4:3992159..4258220hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38266088
hg19266088
hg18266062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5090n100
Supporting Variantsnssv3616164
Samples
Known GenesFAM86EP, OTOP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014368
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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