A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095601



Internal ID22004834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287062..36287062hg38UCSC Ensembl
chr11:36308612..36308612hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597451
Samples
Known GenesCOMMD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095601
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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