A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556616



Internal ID21880971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55982636..55982973hg38UCSC Ensembl
chr5:55278464..55278801hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000349
Supporting Variants
Samples
Known GenesIL6ST
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556616
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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