A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674825



Internal ID15411477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134505414hg38UCSC Ensembl
Innerchr11:134349754..134375308hg19UCSC Ensembl
Innerchr11:133854964..133880518hg18UCSC Ensembl
Innerchr11:133854964..133880518hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3825555
hg1925555
hg1825555
hg1725555
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674825
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