A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569840



Internal ID16357249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71184443..71185709hg38UCSC Ensembl
Innerchr15:71476782..71478048hg19UCSC Ensembl
Innerchr15:69263836..69265102hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381267
hg191267
hg181267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844449, nssv844448
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569840
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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