A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091326



Internal ID22000559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57593179..57593179hg38UCSC Ensembl
chr15:57885377..57885377hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613655
Samples
Known GenesGCOM1, MYZAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091326
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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