A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549081



Internal ID21873436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86021109..86021109hg38UCSC Ensembl
chr4:86942262..86942262hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077271
Supporting Variants
Samples
Known GenesMAPK10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549081
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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