A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955321



Internal ID37524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128146211..128150109hg38UCSC Ensembl
chr4:129067366..129071264hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg383899
hg193899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473331
Supporting Variants
Samples
Known GenesLARP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955321
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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