A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955285



Internal ID37502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127682048..127682048hg38UCSC Ensembl
chr4:128603203..128603203hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549069
Supporting Variants
Samples
Known GenesINTU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955285
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020514


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