A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433141



Internal ID211867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28752582..28753942hg38UCSC Ensembl
chr1:29079094..29080454hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900465
Samples
Known GenesYTHDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433141
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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