A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738121



Internal ID18689716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4190525hg38UCSC Ensembl
Innerchr4:3885796..4192252hg19UCSC Ensembl
Innerchr4:3855594..4243153hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38306457
hg19306457
hg18387560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003533
Supporting Variants
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)nssv3738121
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer