A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065214



Internal ID19154433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24338821..24413936hg38UCSC Ensembl
Innerchr19:24521623..24596738hg19UCSC Ensembl
Innerchr19:24313463..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3875116
hg1975116
hg1875116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3492n100
Supporting Variantsnssv3570778, nssv3570776, nssv3570772, nssv3570781, nssv3570774, nssv3570777, nssv3570775, nssv3570779, nssv3570773, nssv3570780, nssv3570782
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)nsv1065214
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer