A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573253



Internal ID18871534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53425499..53511924hg38UCSC Ensembl
Innerchr19:53928752..54015178hg19UCSC Ensembl
Innerchr19:58620564..58706990hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3886426
hg1986427
hg1886427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065911
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573253
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