A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701791



Internal ID15438443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56563070..56599201hg38UCSC Ensembl
Innerchr11:56330546..56366677hg19UCSC Ensembl
Innerchr11:56087122..56123253hg18UCSC Ensembl
Innerchr11:56087122..56123253hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3836132
hg1936132
hg1836132
hg1736132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525637
Supporting Variants
Samples
Known GenesOR5M10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701791
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