A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054053



Internal ID19143272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5766838..5788096hg38UCSC Ensembl
Innerchr11:5788068..5809326hg19UCSC Ensembl
Innerchr11:5744644..5765902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821259
hg1921259
hg1821259
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1049n100
Supporting Variantsnssv3503171, nssv3707485
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054053
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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