A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518207



Internal ID15098814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11670846..11695677hg38UCSC Ensembl
Innerchr18:11670845..11695676hg19UCSC Ensembl
Innerchr18:11660845..11685676hg18UCSC Ensembl
Innerchr18:11660845..11685676hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3824832
hg1924832
hg1824832
hg1724832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695631
Samples
Known GenesGNAL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518207
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