A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694777



Internal ID15084743
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 StatusS
Merged Variantsnsv522008
Supporting Variants
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)nssv694777
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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