A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449636



Internal ID227868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28862540..28866935hg38UCSC Ensembl
chr2:29085406..29089801hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg384396
hg194396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911364
Samples
Known GenesTRMT61B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449636
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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