A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569339



Internal ID16356748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48929394..48950608hg38UCSC Ensembl
Innerchr15:49221591..49242805hg19UCSC Ensembl
Innerchr15:47008883..47030097hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3821215
hg1921215
hg1821215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842498
Samples
Known GenesSHC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569339
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