A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097351



Internal ID22006584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120169214..120169214hg38UCSC Ensembl
chr11:120039922..120039922hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097351
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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