A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563746



Internal ID21888101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167297446..167302753hg38UCSC Ensembl
chr5:166724451..166729758hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385308
hg195308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016902
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563746
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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