A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518860



Internal ID15446153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32003817..32005026hg38UCSC Ensembl
Innerchr4:32005439..32006648hg19UCSC Ensembl
Innerchr4:31649337..31650546hg18UCSC Ensembl
Innerchr4:31795508..31796717hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
hg171210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696315
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518860
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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