A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726090



Internal ID18677685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62269842..62341216hg38UCSC Ensembl
Innerchr18:59937075..60008449hg19UCSC Ensembl
Innerchr18:58088055..58159429hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3871375
hg1971375
hg1871375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055910
Supporting Variants
Samples
Known GenesKIAA1468, TNFRSF11A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726090
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