A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011861



Internal ID18754396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4183883hg38UCSC Ensembl
Innerchr4:3885796..4185610hg19UCSC Ensembl
Innerchr4:3855594..4236511hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38299815
hg19299815
hg18380918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5085n100
Supporting Variantsnssv3738115, nssv3738116
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011861
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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