A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039936



Internal ID94345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102628867..102628870hg38UCSC Ensembl
chr10:104388624..104388627hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400835
Supporting Variants
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039936
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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