A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523709



Internal ID15451002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4455469..4518847hg38UCSC Ensembl
Innerchr11:4476699..4540077hg19UCSC Ensembl
Innerchr11:4433275..4496653hg18UCSC Ensembl
Innerchr11:4433275..4496653hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863379
hg1963379
hg1863379
hg1763379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv55n21
Supporting Variantsnssv699520
Samples
Known GenesOR52K1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523709
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