A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040699



Internal ID94842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116668059..116733013hg38UCSC Ensembl
chr10:118427570..118492524hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3864955
hg1964955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499342
Supporting Variants
Samples
Known GenesC10orf82, HSPA12A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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