A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565363



Internal ID18863644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43395089..43532709hg38UCSC Ensembl
Innerchr18:40975054..41112674hg19UCSC Ensembl
Innerchr18:39229052..39366672hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38137621
hg19137621
hg18137621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060110
Supporting Variants
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)nssv3565363
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