A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053669



Internal ID19142888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84589903..84671427hg38UCSC Ensembl
Innerchr11:84300946..84382470hg19UCSC Ensembl
Innerchr11:83978594..84060118hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3881525
hg1981525
hg1881525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520126
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)nsv1053669
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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