A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144023



Internal ID343225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3096923..3097167hg38UCSC Ensembl
chr11:3118153..3118397hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042139
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144023
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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