A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410875



Internal ID190190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6397519..6397533hg38UCSC Ensembl
chr5:6397632..6397646hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410875
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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