A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003341



Internal ID18745873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47605279..47649975hg38UCSC Ensembl
Innerchr4:47607296..47651992hg19UCSC Ensembl
Innerchr4:47302053..47346749hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3844697
hg1944697
hg1844697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625132
Samples
Known GenesCORIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003341
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