A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520799



Internal ID15101406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55353463..55468324hg38UCSC Ensembl
Innerchr15:55645661..55760522hg19UCSC Ensembl
Innerchr15:53432953..53547814hg18UCSC Ensembl
Innerchr15:53432953..53547814hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38114862
hg19114862
hg18114862
hg17114862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697618
Samples
Known GenesC15orf65, CCPG1, DYX1C1, DYX1C1-CCPG1, MIR628, PIGB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520799
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