A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293926



Internal ID20503144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69491108..69491108hg38UCSC Ensembl
chr17:67487249..67487249hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763098
Supporting Variants
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293926
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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