A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554868



Internal ID15995591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55660224hg38UCSC Ensembl
Innerchr11:55370325..55427700hg19UCSC Ensembl
Innerchr11:55126901..55184276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3857376
hg1957376
hg1857376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv775930, nssv775929, nssv775933, nssv775931, nssv775932
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554868
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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