A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951151



Internal ID34792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56978522..56978535hg38UCSC Ensembl
chr4:57844688..57844701hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951151
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.056978


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