A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038552



Internal ID93438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76336152..76336171hg38UCSC Ensembl
chr10:78095910..78095929hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544029
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038552
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.142835


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