A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067379



Internal ID18809910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25374848..25612604hg38UCSC Ensembl
Innerchr20:25355484..25593240hg19UCSC Ensembl
Innerchr20:25303484..25541240hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38237757
hg19237757
hg18237757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584681
Samples
Known GenesABHD12, GINS1, NINL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067379
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer