A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564040



Internal ID18862321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1907315..1986262hg38UCSC Ensembl
Innerchr18:1907316..1986263hg19UCSC Ensembl
Innerchr18:1897316..1976263hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3878948
hg1978948
hg1878948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063610
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564040
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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