A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019110



Internal ID19108328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132796614..133105768hg38UCSC Ensembl
Innerchr4:133717769..134026923hg19UCSC Ensembl
Innerchr4:133937219..134246373hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38309155
hg19309155
hg18309155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639523
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019110
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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