A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544919



Internal ID21869274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137538125..137538187hg38UCSC Ensembl
chr4:138459279..138459341hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544919
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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