A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552532



Internal ID21876887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140816018..140828265hg38UCSC Ensembl
chr4:141737172..141749419hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812248
hg1912248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995379
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552532
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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