A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447214



Internal ID225525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132388811..132390820hg38UCSC Ensembl
chr3:132107655..132109664hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382010
hg192010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447214
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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