A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542361



Internal ID316788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192518090..192518121hg38UCSC Ensembl
chr1:192487220..192487251hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16893825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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