A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447735



Internal ID226028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186325854..186345998hg38UCSC Ensembl
chr2:187190581..187210725hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3820145
hg1920145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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