A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647011



Internal ID18945292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109932371..110028680hg38UCSC Ensembl
Innerchr5:109268072..109364381hg19UCSC Ensembl
Innerchr5:109295971..109392280hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3896310
hg1996310
hg1896310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030510
Supporting Variants
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)nssv3647011
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