A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528190



Internal ID15108797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58569147..58580292hg38UCSC Ensembl
Innerchr11:58336620..58347765hg19UCSC Ensembl
Innerchr11:58093196..58104341hg18UCSC Ensembl
Innerchr11:58093196..58104341hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811146
hg1911146
hg1811146
hg1711146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704747
Samples
Known GenesLPXN, ZFP91, ZFP91-CNTF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528190
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