A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556520



Internal ID15997243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125207472..125212568hg38UCSC Ensembl
Innerchr11:125077368..125082464hg19UCSC Ensembl
Innerchr11:124582578..124587674hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385097
hg195097
hg185097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2193n54
Supporting Variantsnssv784702
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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