A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035138



Internal ID18777669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6607812..6980555hg38UCSC Ensembl
Innerchr11:6629042..7001786hg19UCSC Ensembl
Innerchr11:6585618..6958362hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38372744
hg19372745
hg18372745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503487
Samples
Known GenesDCHS1, GVINP1, ILK, MRPL17, OR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR2D2, OR2D3, OR6A2, TAF10, TPP1, ZNF215
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035138
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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