A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085575



Internal ID21994808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87304461..87304461hg38UCSC Ensembl
chr11:87015503..87015503hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580322
Samples
Known GenesTMEM135
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085575
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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