A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050013



Internal ID18792544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58627125..59453617hg38UCSC Ensembl
Innerchr11:58394598..59221090hg19UCSC Ensembl
Innerchr11:58151174..58977666hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38826493
hg19826493
hg18826493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519306
Samples
Known GenesDTX4, FAM111A, FAM111B, GLYAT, GLYATL1, GLYATL2, LOC283194, MPEG1, OR5A1, OR5A2, OR5AN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050013
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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