A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898582



Internal ID15845852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34481093..34482608hg38UCSC Ensembl
Innerchr19:34971998..34973513hg19UCSC Ensembl
Innerchr19:39663838..39665353hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381516
hg191516
hg181516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579351
Supporting Variants
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898582
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