A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554830



Internal ID15995553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55656731hg38UCSC Ensembl
Innerchr11:55367889..55424207hg19UCSC Ensembl
Innerchr11:55124465..55180783hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3856319
hg1956319
hg1856319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv775230, nssv775231, nssv775229
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)nsv554830
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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