A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427341



Internal ID22485211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158701175..158701448hg38UCSC Ensembl
chr6:159122207..159122480hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900118
Supporting Variants
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427341
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.34


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