A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461829



Internal ID239772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169759877..169762701hg38UCSC Ensembl
chr4:170681028..170683852hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg382825
hg192825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461829
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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