A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039328



Internal ID93941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119544334..119544385hg38UCSC Ensembl
chr10:121303846..121303897hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039328
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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