A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421556



Internal ID200624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33180860..33180986hg38UCSC Ensembl
chr1:33646461..33646587hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901393
Samples
Known GenesTRIM62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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