A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085895



Internal ID21995128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101143094..101143094hg38UCSC Ensembl
chr11:101013825..101013825hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587253
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085895
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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