A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956361



Internal ID38212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141581454..141582698hg38UCSC Ensembl
chr4:142502607..142503851hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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