A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520017



Internal ID15447310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38109249..38125842hg38UCSC Ensembl
Innerchr11:38130799..38147392hg19UCSC Ensembl
Innerchr11:38087375..38103968hg18UCSC Ensembl
Innerchr11:38087375..38103968hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3816594
hg1916594
hg1816594
hg1716594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697179
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520017
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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