A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440144



Internal ID218660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96063643..96066468hg38UCSC Ensembl
chr3:95782487..95785312hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382826
hg192826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440144
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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