A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057869



Internal ID18800400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12454882..12593969hg38UCSC Ensembl
Innerchr19:12565696..12704783hg19UCSC Ensembl
Innerchr19:12426696..12565783hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38139088
hg19139088
hg18139088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3436n100
Supporting Variantsnssv3564769
Samples
Known GenesZNF490, ZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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