A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448208



Internal ID226489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:126874413..126883597hg38UCSC Ensembl
chr2:127631989..127641173hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg389185
hg199185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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