A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569502



Internal ID16356911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54406999..54495160hg38UCSC Ensembl
Innerchr15:54699197..54787358hg19UCSC Ensembl
Innerchr15:52486489..52574650hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3888162
hg1988162
hg1888162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4541n54
Supporting Variantsnssv843291
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569502
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