A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060866



Internal ID18803397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4454150..4494321hg38UCSC Ensembl
Innerchr18:4454150..4494321hg19UCSC Ensembl
Innerchr18:4444150..4484321hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3840172
hg1940172
hg1840172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3316n100
Supporting Variantsnssv3564073
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060866
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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