A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450035



Internal ID228254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206124279..206126488hg38UCSC Ensembl
chr2:206989003..206991212hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922977
Samples
Known GenesNDUFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450035
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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