A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526402



Internal ID15453695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68433827..68449952hg38UCSC Ensembl
Innerchr11:68201295..68217420hg19UCSC Ensembl
Innerchr11:67957871..67973996hg18UCSC Ensembl
Innerchr11:67957871..67973996hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3816126
hg1916126
hg1816126
hg1716126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv73n21
Supporting Variantsnssv702701
Samples
Known GenesLRP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526402
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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