A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564698



Internal ID18516293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11804370..11950569hg38UCSC Ensembl
Innerchr19:11915185..12061384hg19UCSC Ensembl
Innerchr19:11776185..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38146200
hg19146200
hg18146200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057762
Supporting Variants
Samples
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564698
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