A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521623



Internal ID15102230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134307381..134756993hg38UCSC Ensembl
Innerchr11:134177275..134626887hg19UCSC Ensembl
Innerchr11:133682485..134132097hg18UCSC Ensembl
Innerchr11:133682485..134132097hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38449613
hg19449613
hg18449613
hg17449613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694467
Samples
Known GenesB3GAT1, GLB1L2, GLB1L3, LOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521623
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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