A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449477



Internal ID227711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96340913..96351522hg38UCSC Ensembl
chr3:96059757..96070366hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810610
hg1910610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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