A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950024



Internal ID34029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51851316..51851441hg38UCSC Ensembl
chr4:52717482..52717607hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460781
Supporting Variants
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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