A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959267



Internal ID40155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173488241..173492528hg38UCSC Ensembl
chr4:174409392..174413679hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg384288
hg194288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959267
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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