A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026100



Internal ID21935443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65123940..65124031hg38UCSC Ensembl
chr11:64891412..64891503hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589950
Samples
Known GenesMRPL49
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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