A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441665



Internal ID220128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102106161..102115105hg38UCSC Ensembl
chr3:101825005..101833949hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg388945
hg198945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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