A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421898



Internal ID200958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102768049..102838032hg38UCSC Ensembl
chr1:103233605..103303588hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3869984
hg1969984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421898
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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