A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580094



Internal ID16020817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53429042..53502054hg38UCSC Ensembl
Innerchr19:53932295..54005308hg19UCSC Ensembl
Innerchr19:58624107..58697120hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3873013
hg1973014
hg1873014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n54
Supporting Variantsnssv1150168
SamplesHGDP00699
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580094
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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