A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570834



Internal ID16358243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101239889..101252467hg38UCSC Ensembl
Innerchr15:101780094..101792672hg19UCSC Ensembl
Innerchr15:99597617..99610195hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3812579
hg1912579
hg1812579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4789n54
Supporting Variantsnssv851026
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570834
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