A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17683791



Internal ID107457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79399328..79408940hg38UCSC Ensembl
chr10:81159084..81168696hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389613
hg199613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485598
Supporting Variants
Samples
Known GenesZCCHC24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17683791
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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