A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049887



Internal ID18792418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75226932..75329394hg38UCSC Ensembl
Innerchr11:74937977..75040438hg19UCSC Ensembl
Innerchr11:74615625..74718086hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38102463
hg19102462
hg18102462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1225n100
Supporting Variantsnssv3710658
Samples
Known GenesARRB1, TPBGL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049887
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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