A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088828



Internal ID21998061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74687954..74687954hg38UCSC Ensembl
chr16:74721852..74721852hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637401
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088828
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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