A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422197



Internal ID201246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24017085..24023271hg38UCSC Ensembl
chr1:24343575..24349761hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386187
hg196187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n206
Supporting Variantsnssv16901154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422197
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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