A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958677



Internal ID39756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156203194..156203194hg38UCSC Ensembl
chr4:157124346..157124346hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958677
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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