A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450736



Internal ID228935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3906535..4082304hg38UCSC Ensembl
chr3:3948219..4123988hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38175770
hg19175770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv336n206
Supporting Variantsnssv16929932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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