A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064114



Internal ID19153333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43756208..44178649hg38UCSC Ensembl
Innerchr18:41336173..41758614hg19UCSC Ensembl
Innerchr18:39590171..40012612hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38422442
hg19422442
hg18422442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565367
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)nsv1064114
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