A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554888



Internal ID15995611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55641224hg38UCSC Ensembl
Innerchr11:55371021..55408700hg19UCSC Ensembl
Innerchr11:55127597..55165276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3837680
hg1937680
hg1837680
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1912n54
Supporting Variantsnssv775983, nssv775987, nssv775986, nssv775981, nssv775984, nssv775982, nssv775985
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554888
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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