A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554019



Internal ID21878374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182932677..182932677hg38UCSC Ensembl
chr4:183853830..183853830hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554019
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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