A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582552



Internal ID16369961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102012099..102014233hg38UCSC Ensembl
Innerchr2:102628561..102630695hg19UCSC Ensembl
Innerchr2:101994993..101997127hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382135
hg192135
hg182135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914699
Samples
Known GenesIL1R2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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