A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552825



Internal ID15993548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:412505..431554hg38UCSC Ensembl
Innerchr11:412505..431554hg19UCSC Ensembl
Innerchr11:402505..421554hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819050
hg1919050
hg1819050
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763440, nssv763439
Samples
Known GenesANO9, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552825
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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