A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013723



Internal ID19102942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3912156..4081209hg38UCSC Ensembl
Innerchr4:3913883..4082936hg19UCSC Ensembl
Innerchr4:3964803..4133837hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38169054
hg19169054
hg18169035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5088n100
Supporting Variantsnssv3738135
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)nsv1013723
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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