A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054310



Internal ID19143529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84950637..84991679hg38UCSC Ensembl
Innerchr11:84661681..84702723hg19UCSC Ensembl
Innerchr11:84339329..84380371hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3841043
hg1941043
hg1841043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516704
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)nsv1054310
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