A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519819



Internal ID15100426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43410496..43451557hg38UCSC Ensembl
Innerchr11:43432046..43473107hg19UCSC Ensembl
Innerchr11:43388622..43429683hg18UCSC Ensembl
Innerchr11:43388622..43429683hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3841062
hg1941062
hg1841062
hg1741062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694348
Samples
Known GenesTTC17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519819
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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