A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444106



Internal ID222488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16738094..16738147hg38UCSC Ensembl
chr2:16919361..16919414hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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