A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515973



Internal ID15443030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75858222..76121271hg38UCSC Ensembl
Innerchr11:75569267..75832315hg19UCSC Ensembl
Innerchr11:75246915..75509963hg18UCSC Ensembl
Innerchr11:75246915..75509963hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38263050
hg19263049
hg18263049
hg17263049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665555, nssv703792, nssv694527, nssv657132, nssv680167
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515973
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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