A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561921



Internal ID334887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32910144..32910195hg38UCSC Ensembl
chr1:33375745..33375796hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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