A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542226



Internal ID21866581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69523197..69524527hg38UCSC Ensembl
chr4:70388915..70390245hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542226
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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