A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447908



Internal ID226198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101288028..101288082hg38UCSC Ensembl
chr3:101006872..101006926hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734904
Samples
Known GenesIMPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447908
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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