A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026674



Internal ID21936017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3128145..3129034hg38UCSC Ensembl
chr11:3149375..3150264hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592854
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026674
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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