A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451896



Internal ID230063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10440869..10441507hg38UCSC Ensembl
chr2:10580995..10581633hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910006
Samples
Known GenesODC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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