A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528806



Internal ID15456099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166471277..166479481hg38UCSC Ensembl
Innerchr6:166884765..166892969hg19UCSC Ensembl
Innerchr6:166804755..166812959hg18UCSC Ensembl
Innerchr6:166855176..166863380hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388205
hg198205
hg188205
hg178205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv400n21
Supporting Variantsnssv705480
Samples
Known GenesRPS6KA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528806
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