A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672789



Internal ID15062755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55628565..55674892hg38UCSC Ensembl
Innerchr11:55396041..55442368hg19UCSC Ensembl
Innerchr11:55152617..55198944hg18UCSC Ensembl
Innerchr11:55152617..55198944hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3846328
hg1946328
hg1846328
hg1746328
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672789
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