A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554885



Internal ID15995608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55631424hg38UCSC Ensembl
Innerchr11:55371021..55398900hg19UCSC Ensembl
Innerchr11:55127597..55155476hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3827880
hg1927880
hg1827880
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1919n54
Supporting Variantsnssv775974, nssv775975, nssv775973, nssv775972
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554885
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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