A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451444



Internal ID229626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5539920..5540025hg38UCSC Ensembl
chr2:5680052..5680157hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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