A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060601



Internal ID19149820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64086577..64131053hg38UCSC Ensembl
Innerchr20:62717930..62762406hg19UCSC Ensembl
Innerchr20:62188374..62232850hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844477
hg1944477
hg1844477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4346n100
Supporting Variantsnssv3584505
Samples
Known GenesNPBWR2, OPRL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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