A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038978



Internal ID18781509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234887..4368359hg38UCSC Ensembl
Innerchr11:4256117..4389589hg19UCSC Ensembl
Innerchr11:4212693..4346165hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38133473
hg19133473
hg18133473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1022n100
Supporting Variantsnssv3522369, nssv3511062
Samples
Known GenesOR52B4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038978
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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