A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428624



Internal ID207490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25819437..25819505hg38UCSC Ensembl
chr1:26145928..26145996hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428624
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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