A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949492



Internal ID33676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67532169..67532859hg38UCSC Ensembl
chr4:68397887..68398577hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466902
Supporting Variants
Samples
Known GenesCENPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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