A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040961



Internal ID95023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103583767..103583767hg38UCSC Ensembl
chr10:105343524..105343524hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553442
Supporting Variants
Samples
Known GenesNEURL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.202797


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