A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061025



Internal ID18803556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5012384..5228283hg38UCSC Ensembl
Innerchr18:5012383..5228282hg19UCSC Ensembl
Innerchr18:5002383..5218282hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38215900
hg19215900
hg18215900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3317n100
Supporting Variantsnssv3725277
Samples
Known GenesC18orf42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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