A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893545



Internal ID15840815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10102342..10103231hg38UCSC Ensembl
Innerchr19:10213018..10213907hg19UCSC Ensembl
Innerchr19:10074018..10074907hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38890
hg19890
hg18890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578611
Supporting Variants
Samples
Known GenesANGPTL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893545
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