A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036827



Internal ID21946170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126568115..126569049hg38UCSC Ensembl
chr11:126438010..126438944hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616541
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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