A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059494



Internal ID18802025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25396966..25461199hg38UCSC Ensembl
Innerchr20:25377602..25441835hg19UCSC Ensembl
Innerchr20:25325602..25389835hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3864234
hg1964234
hg1864234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737181
Samples
Known GenesGINS1, NINL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059494
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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