A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554881



Internal ID15995604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55627975hg38UCSC Ensembl
Innerchr11:55371021..55395451hg19UCSC Ensembl
Innerchr11:55127597..55152027hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3824431
hg1924431
hg1824431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n54
Supporting Variantsnssv775964
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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