A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090795



Internal ID22000028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1754526..1754526hg38UCSC Ensembl
chr11:1775756..1775756hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596183
Samples
Known GenesCTSD, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090795
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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