A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579336



Internal ID16020059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33621709..33622309hg38UCSC Ensembl
Innerchr19:34112615..34113215hg19UCSC Ensembl
Innerchr19:38804455..38805055hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38601
hg19601
hg18601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6406n54
Supporting Variantsnssv898545, nssv898544
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579336
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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