A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700026



Internal ID15089992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45770426..45972404hg38UCSC Ensembl
Innerchr1:46236098..46438076hg19UCSC Ensembl
Innerchr1:46008685..46210663hg18UCSC Ensembl
Innerchr1:45948118..46150096hg17UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38201979
hg19201979
hg18201979
hg17201979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524147
Supporting Variants
Samples
Known GenesMAST2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700026
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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