A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039769



Internal ID94233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97608554..97610555hg38UCSC Ensembl
chr10:99368311..99370312hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479729
Supporting Variants
Samples
Known GenesHOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039769
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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