A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878449



Internal ID15825719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14105924..14540311hg38UCSC Ensembl
Innerchr18:14105923..14540310hg19UCSC Ensembl
Innerchr18:14095923..14530310hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38434388
hg19434388
hg18434388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576531
Supporting Variants
Samples
Known GenesANKRD20A5P, CXADRP3, CYP4F35P, POTEC, ZNF519
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878449
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