A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv890296



Internal ID15837566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80071200..80073417hg38UCSC Ensembl
Innerchr18:77831200..77831830hg19UCSC Ensembl
Innerchr18:75932188..75932818hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382218
hg19631
hg18631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577961
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)nssv890296
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