A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464751



Internal ID242622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21846981..21847162hg38UCSC Ensembl
chr6:21847212..21847393hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982261
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464751
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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