A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421271



Internal ID200354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31176383..31176434hg38UCSC Ensembl
chr1:31649230..31649281hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421271
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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