A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036041



Internal ID91769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49157585..49171501hg38UCSC Ensembl
chr10:50365630..50379546hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3813917
hg1913917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479668
Supporting Variants
Samples
Known GenesC10orf128
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036041
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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