A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552766



Internal ID16340175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:248181..285936hg38UCSC Ensembl
Innerchr11:248181..285936hg19UCSC Ensembl
Innerchr11:238181..275936hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3837756
hg1937756
hg1837756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763049
Samples
Known GenesNLRP6, PSMD13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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