A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948056



Internal ID32731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37877778..37879936hg38UCSC Ensembl
chr4:37879399..37881557hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948056
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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