A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526604



Internal ID15107211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113014359..113057442hg38UCSC Ensembl
Innerchr11:112885081..112928164hg19UCSC Ensembl
Innerchr11:112390291..112433374hg18UCSC Ensembl
Innerchr11:112390291..112433374hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3843084
hg1943084
hg1843084
hg1743084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702924
Samples
Known GenesNCAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526604
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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