A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466902



Internal ID244728
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 StatusM
Merged Variants
Supporting Variantsnssv16949492
Samples
Known GenesCENPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466902
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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