A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701879



Internal ID15091845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55655110..55679951hg38UCSC Ensembl
Innerchr11:55422586..55447427hg19UCSC Ensembl
Innerchr11:55179162..55204003hg18UCSC Ensembl
Innerchr11:55179162..55204003hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3824842
hg1924842
hg1824842
hg1724842
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701879
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