A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061902



Internal ID18804433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15171818..15186765hg38UCSC Ensembl
Innerchr19:15282629..15297576hg19UCSC Ensembl
Innerchr19:15143629..15158576hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3814948
hg1914948
hg1814948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3440n100
Supporting Variantsnssv3564786, nssv3723290
Samples
Known GenesMIR6795, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061902
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