A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033989



Internal ID90358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62407876..62413716hg38UCSC Ensembl
chr10:64167635..64173475hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480660
Supporting Variants
Samples
Known GenesZNF365
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002186


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