A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036924



Internal ID92372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91792651..91794129hg38UCSC Ensembl
chr10:93552408..93553886hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487734
Supporting Variants
Samples
Known GenesTNKS2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036924
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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