A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442892



Internal ID221303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96588470..96608315hg38UCSC Ensembl
chr3:96307314..96327159hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3819846
hg1919846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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