A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527072



Internal ID15454365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121577381..121615843hg38UCSC Ensembl
Innerchr11:121448090..121486552hg19UCSC Ensembl
Innerchr11:120953300..120991762hg18UCSC Ensembl
Innerchr11:120953300..120991762hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3838463
hg1938463
hg1838463
hg1738463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703451
Samples
Known GenesSORL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527072
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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