A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705839



Internal ID15442491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121486259..121565561hg38UCSC Ensembl
Innerchr11:121356968..121436270hg19UCSC Ensembl
Innerchr11:120862178..120941480hg18UCSC Ensembl
Innerchr11:120862178..120941480hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3879303
hg1979303
hg1879303
hg1779303
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522474
Supporting Variants
Samples
Known GenesSORL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705839
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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