A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956673



Internal ID38420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126205210..126210463hg38UCSC Ensembl
chr4:127126365..127131618hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg385254
hg195254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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