A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040419



Internal ID19129638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84483784..84576532hg38UCSC Ensembl
Innerchr11:84194827..84287575hg19UCSC Ensembl
Innerchr11:83872475..83965223hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3892749
hg1992749
hg1892749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507656
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040419
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