A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065211



Internal ID19154430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39808481..39846180hg38UCSC Ensembl
Innerchr18:37388445..37426144hg19UCSC Ensembl
Innerchr18:35642443..35680142hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3837700
hg1937700
hg1837700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725319
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)nsv1065211
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