A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035740



Internal ID18778271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1264737..1374743hg38UCSC Ensembl
Innerchr11:1285967..1395973hg19UCSC Ensembl
Innerchr11:1242543..1352549hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38110007
hg19110007
hg18110007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1014n100
Supporting Variantsnssv3504098
Samples
Known GenesTOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035740
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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