A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668532



Internal ID15058498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134288851..134340635hg38UCSC Ensembl
Innerchr11:134158745..134210529hg19UCSC Ensembl
Innerchr11:133663955..133715739hg18UCSC Ensembl
Innerchr11:133663955..133715739hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3851785
hg1951785
hg1851785
hg1751785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516459
Supporting Variants
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668532
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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