A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528491



Internal ID15455784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85013751..85183989hg38UCSC Ensembl
Innerchr11:84724795..84895033hg19UCSC Ensembl
Innerchr11:84402443..84572681hg18UCSC Ensembl
Innerchr11:84402443..84572681hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38170239
hg19170239
hg18170239
hg17170239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv75n21
Supporting Variantsnssv705096
Samples
Known GenesDLG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528491
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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