A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066008



Internal ID19155227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10081421..10098150hg38UCSC Ensembl
Innerchr18:10081418..10098147hg19UCSC Ensembl
Innerchr18:10071418..10088147hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3816730
hg1916730
hg1816730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564100
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)nsv1066008
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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