A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065571



Internal ID19154790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27550236hg38UCSC Ensembl
Innerchr19:27747981..28041144hg19UCSC Ensembl
Innerchr19:32439821..32732984hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38293164
hg19293164
hg18293164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3571989
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)nsv1065571
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