A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954533



Internal ID37013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055502..121055648hg38UCSC Ensembl
chr4:121976657..121976803hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464890
Supporting Variants
Samples
Known GenesNDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009054


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