A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049277



Internal ID19138496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4926930..4952787hg38UCSC Ensembl
Innerchr11:4948160..4974017hg19UCSC Ensembl
Innerchr11:4904736..4930593hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825858
hg1925858
hg1825858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1027n100
Supporting Variantsnssv3515810
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)nsv1049277
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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