A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025398



Internal ID21934741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5986471..5986647hg38UCSC Ensembl
chr11:6007701..6007877hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583700
Samples
Known GenesOR52L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025398
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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