A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435691



Internal ID214327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208255468..208261451hg38UCSC Ensembl
chr2:209120192..209126175hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg385984
hg195984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928052
Samples
Known GenesIDH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435691
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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