A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058830



Internal ID18801361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4663154..4725219hg38UCSC Ensembl
Innerchr20:4643800..4705865hg19UCSC Ensembl
Innerchr20:4591800..4653865hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3862066
hg1962066
hg1862066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599351
Samples
Known GenesPRND, PRNP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058830
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