A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526297



Internal ID15106904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7665443..7666484hg38UCSC Ensembl
Innerchr11:7686674..7687715hg19UCSC Ensembl
Innerchr11:7643250..7644291hg18UCSC Ensembl
Innerchr11:7643250..7644291hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381042
hg191042
hg181042
hg171042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702578
Samples
Known GenesCYB5R2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526297
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