A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948961



Internal ID33328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55150199..55150245hg38UCSC Ensembl
chr4:56016366..56016412hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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