A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445539



Internal ID223886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185562137..185571574hg38UCSC Ensembl
chr3:185279925..185289362hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg389438
hg199438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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