A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896163



Internal ID16190119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20164238..20315194hg38UCSC Ensembl
Innerchr19:20275047..20426003hg19UCSC Ensembl
Innerchr19:20136047..20287003hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38150957
hg19150957
hg18150957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578806
Supporting Variants
Samples
Known GenesZNF486
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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