A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036407



Internal ID18778938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1264737..1397647hg38UCSC Ensembl
Innerchr11:1285967..1418877hg19UCSC Ensembl
Innerchr11:1242543..1375453hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38132911
hg19132911
hg18132911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1014n100
Supporting Variantsnssv3706388
Samples
Known GenesBRSK2, TOLLIP, 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)nsv1036407
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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