A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941192



Internal ID28168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151685749..151701587hg38UCSC Ensembl
chr3:151403537..151419375hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3815839
hg1915839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435026
Supporting Variants
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941192
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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