A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554006



Internal ID16341415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36610965..37150283hg38UCSC Ensembl
Innerchr11:36632515..37171833hg19UCSC Ensembl
Innerchr11:36589091..37128409hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38539319
hg19539319
hg18539319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771063
Samples
Known GenesC11orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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