A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038617



Internal ID93484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79394531..79395804hg38UCSC Ensembl
chr10:81154287..81155560hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485205
Supporting Variants
Samples
Known GenesZCCHC24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038617
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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