A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16943687



Internal ID29770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180130003..180135034hg38UCSC Ensembl
chr3:179847791..179852822hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385032
hg195032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16943687
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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