A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv890311



Internal ID15837581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80071200..80074823hg38UCSC Ensembl
Innerchr18:77831200..77833127hg19UCSC Ensembl
Innerchr18:75932188..75934115hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383624
hg191928
hg181928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577962
Supporting Variants
Samples
Known GenesRBFADN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv890311
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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