A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958877



Internal ID39891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158484526..158484577hg38UCSC Ensembl
chr4:159405678..159405729hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410670
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958877
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007337


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