A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022557



Internal ID21931900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3113211..3115091hg38UCSC Ensembl
chr11:3134441..3136321hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593404
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022557
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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