A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544084



Internal ID21868439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190122717..190122717hg38UCSC Ensembl
chr4:191043872..191043872hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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