A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059447



Internal ID18801978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25961292..26324931hg38UCSC Ensembl
Innerchr20:25941928..26305567hg19UCSC Ensembl
Innerchr20:25889928..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38363640
hg19363640
hg18363640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4292n100
Supporting Variantsnssv3584686
Samples
Known GenesFAM182A, LOC100134868, LOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059447
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