A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554392



Internal ID15995115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49824008..50098683hg38UCSC Ensembl
Innerchr11:49845560..50057854hg19UCSC Ensembl
Innerchr11:49802136..50014430hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38274676
hg19212295
hg18212295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1813n54
Supporting Variantsnssv1174300
Samples1780854511_A
Known GenesOR4C12, OR4C13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554392
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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