A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064925



Internal ID19154144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19062130..19098649hg38UCSC Ensembl
Innerchr20:19042774..19079293hg19UCSC Ensembl
Innerchr20:18990774..19027293hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3836520
hg1936520
hg1836520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737172, nssv3737171
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064925
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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