A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032736



Internal ID89518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43167355..43167404hg38UCSC Ensembl
chr10:43662803..43662852hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537774
Supporting Variants
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013737


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