A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552823



Internal ID15993546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:409592..412359hg38UCSC Ensembl
Innerchr11:409592..412359hg19UCSC Ensembl
Innerchr11:399592..402359hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382768
hg192768
hg182768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763437
Samples
Known GenesSIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552823
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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