A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060972



Internal ID19150191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27704107hg38UCSC Ensembl
Innerchr19:27747981..28195015hg19UCSC Ensembl
Innerchr19:32439821..32886855hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38447035
hg19447035
hg18447035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3499n100
Supporting Variantsnssv3572037
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)nsv1060972
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