A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524361



Internal ID15104968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7655154..7688219hg38UCSC Ensembl
Innerchr11:7676385..7709450hg19UCSC Ensembl
Innerchr11:7632961..7666026hg18UCSC Ensembl
Innerchr11:7632961..7666026hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833066
hg1933066
hg1833066
hg1733066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv58n21
Supporting Variantsnssv700272
Samples
Known GenesCYB5R2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524361
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