A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008577



Internal ID18751108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4163608hg38UCSC Ensembl
Innerchr4:3885796..4165335hg19UCSC Ensembl
Innerchr4:3855594..4216236hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38279540
hg19279540
hg18360643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5085n100
Supporting Variantsnssv3738110
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)nsv1008577
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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