A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955287



Internal ID37503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127723755..127725197hg38UCSC Ensembl
chr4:128644910..128646352hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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