A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564724



Internal ID18863005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12405336..12434058hg38UCSC Ensembl
Innerchr19:12516150..12544872hg19UCSC Ensembl
Innerchr19:12377150..12405872hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3828723
hg1928723
hg1828723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059474
Supporting Variants
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564724
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