A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554884



Internal ID15995607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55630541hg38UCSC Ensembl
Innerchr11:55371021..55398017hg19UCSC Ensembl
Innerchr11:55127597..55154593hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3826997
hg1926997
hg1826997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n54
Supporting Variantsnssv775970, nssv775971
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554884
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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