A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952049



Internal ID35388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69804931..69804982hg38UCSC Ensembl
chr4:70670649..70670700hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952049
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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