A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540180



Internal ID21864535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61770504..61773085hg38UCSC Ensembl
chr4:62636222..62638803hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg382582
hg192582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997667
Supporting Variants
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540180
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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