A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099115



Internal ID22008348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118581929..118581929hg38UCSC Ensembl
chr11:118452644..118452644hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598386
Samples
Known GenesARCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099115
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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