A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526941



Internal ID15454234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38423218..38437382hg38UCSC Ensembl
Innerchr11:38444768..38458932hg19UCSC Ensembl
Innerchr11:38401344..38415508hg18UCSC Ensembl
Innerchr11:38401344..38415508hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814165
hg1914165
hg1814165
hg1714165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703309
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526941
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