A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564708



Internal ID18862989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12395059..12429064hg38UCSC Ensembl
Innerchr19:12505873..12539878hg19UCSC Ensembl
Innerchr19:12366873..12400878hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3834006
hg1934006
hg1834006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057201
Supporting Variants
Samples
Known GenesZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564708
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