A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587349



Internal ID21779392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54104720..54104836hg38UCSC Ensembl
chr8:55017280..55017396hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587349
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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