A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553564



Internal ID15994287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16197795..16245194hg38UCSC Ensembl
Innerchr11:16219341..16266740hg19UCSC Ensembl
Innerchr11:16175917..16223316hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3847400
hg1947400
hg1847400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1662n54
Supporting Variantsnssv1175077
Samples1780862001_A
Known GenesSOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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