A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061696



Internal ID19150915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24219440..24338821hg38UCSC Ensembl
Innerchr19:24402242..24521623hg19UCSC Ensembl
Innerchr19:24194082..24313463hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38119382
hg19119382
hg18119382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3486n100
Supporting Variantsnssv3570691
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)nsv1061696
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