A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039863



Internal ID94298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101845758..101845809hg38UCSC Ensembl
chr10:103605515..103605566hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557584
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039863
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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