A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518571



Internal ID15099178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49141396..49606281hg38UCSC Ensembl
Innerchr11:49162948..49627833hg19UCSC Ensembl
Innerchr11:49119524..49584409hg18UCSC Ensembl
Innerchr11:49119524..49584409hg17UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38464886
hg19464886
hg18464886
hg17464886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696014
Samples
Known GenesFOLH1, LOC440040
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518571
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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