A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5395841



Internal ID175263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77971924..77971975hg38UCSC Ensembl
chr10:79731682..79731733hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5395841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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