A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413632



Internal ID192922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29526623..29526674hg38UCSC Ensembl
chr1:29853135..29853186hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413632
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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