A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017469



Internal ID18760003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17373274..17416534hg38UCSC Ensembl
Innerchr5:17373383..17416643hg19UCSC Ensembl
Innerchr5:17426383..17469643hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3843261
hg1943261
hg1843261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5578n100
Supporting Variantsnssv3638307, nssv3638308
Samples
Known GenesLOC401177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017469
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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