A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999221



Internal ID18812071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4151021hg38UCSC Ensembl
Innerchr4:3885796..4152748hg19UCSC Ensembl
Innerchr4:3855594..4203649hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38266953
hg19266953
hg18348056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5085n100
Supporting Variantsnssv3738109
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)nsv999221
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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