A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522008



Internal ID15102615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1359746..1657932hg38UCSC Ensembl
Innerchr20:1340390..1638578hg19UCSC Ensembl
Innerchr20:1288390..1586578hg18UCSC Ensembl
Innerchr20:1288390..1586578hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38298187
hg19298189
hg18298189
hg17298189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694777
Samples
Known GenesFKBP1A, FKBP1A-SDCBP2, MIR6869, NSFL1C, SDCBP2-AS1, SIRPB1, SIRPB2, SIRPD, SIRPG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522008
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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