A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526862



Internal ID15454155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:10111994..10121882hg38UCSC Ensembl
Innerchr20:10092642..10102530hg19UCSC Ensembl
Innerchr20:10040642..10050530hg18UCSC Ensembl
Innerchr20:10040642..10050530hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg389889
hg199889
hg189889
hg179889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703220
Samples
Known GenesSNAP25-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526862
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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