A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419409



Internal ID198541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61454370..61454523hg38UCSC Ensembl
chr1:61920042..61920195hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906056
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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