A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657132



Internal ID15393784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75858222..76106192hg38UCSC Ensembl
Innerchr11:75569267..75817236hg19UCSC Ensembl
Innerchr11:75246915..75494884hg18UCSC Ensembl
Innerchr11:75246915..75494884hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38247971
hg19247970
hg18247970
hg17247970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515973
Supporting Variants
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657132
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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