A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088144



Internal ID21997377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26169540..26169540hg38UCSC Ensembl
chr11:26191087..26191087hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088144
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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