A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569409



Internal ID16010132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51736717..51975947hg38UCSC Ensembl
Innerchr15:52028914..52268144hg19UCSC Ensembl
Innerchr15:49816206..50055436hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38239231
hg19239231
hg18239231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842983
Samples
Known GenesLEO1, LYSMD2, TMOD2, TMOD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569409
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