A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706411



Internal ID19004692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4931684..4952787hg38UCSC Ensembl
Innerchr11:4952914..4974017hg19UCSC Ensembl
Innerchr11:4909490..4930593hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821104
hg1921104
hg1821104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044434
Supporting Variants
Samples
Known GenesOR51A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706411
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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