A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449122



Internal ID227369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106368176..106382441hg38UCSC Ensembl
chr3:106087023..106101288hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3814266
hg1914266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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