A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560196



Internal ID21884551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158693752..158693898hg38UCSC Ensembl
chr6:159114784..159114930hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019007
Supporting Variants
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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