A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556533



Internal ID16343942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126760536..126825252hg38UCSC Ensembl
Innerchr11:126630431..126695147hg19UCSC Ensembl
Innerchr11:126135641..126200357hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3864717
hg1964717
hg1864717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784713
Samples
Known GenesKIRREL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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