A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694553



Internal ID118219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96388870..96390845hg38UCSC Ensembl
chr13:97041124..97043099hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505502
Supporting Variants
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694553
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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