A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696869



Internal ID15433521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3145947..3147308hg38UCSC Ensembl
Innerchr11:3167177..3168538hg19UCSC Ensembl
Innerchr11:3123753..3125114hg18UCSC Ensembl
Innerchr11:3123753..3125114hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381362
hg191362
hg181362
hg171362
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519468
Supporting Variants
Samples
Known GenesOSBPL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696869
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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