A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569406



Internal ID16356815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51546522..51598085hg38UCSC Ensembl
Innerchr15:51838719..51890282hg19UCSC Ensembl
Innerchr15:49626011..49677574hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3851564
hg1951564
hg1851564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148865
SamplesNINDS_223
Known GenesDMXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569406
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