A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556532



Internal ID15997255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126728656..126738551hg38UCSC Ensembl
Innerchr11:126598551..126608446hg19UCSC Ensembl
Innerchr11:126103761..126113656hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389896
hg199896
hg189896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784712
Samples
Known GenesKIRREL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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