A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546618



Internal ID21870973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24991340..24993658hg38UCSC Ensembl
chr4:24992962..24995280hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382319
hg192319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546618
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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