A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706074



Internal ID15442726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11404651..11405493hg38UCSC Ensembl
Innerchr11:11426198..11427040hg19UCSC Ensembl
Innerchr11:11382774..11383616hg18UCSC Ensembl
Innerchr11:11382774..11383616hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38843
hg19843
hg18843
hg17843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522669
Supporting Variants
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706074
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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