A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066946



Internal ID19156165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59985406..59997780hg38UCSC Ensembl
Innerchr18:57652638..57665012hg19UCSC Ensembl
Innerchr18:55803618..55815992hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3812375
hg1912375
hg1812375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3368n100
Supporting Variantsnssv3565526, nssv3565524, nssv3565525
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)nsv1066946
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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