A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427741



Internal ID206637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14292728..14295946hg38UCSC Ensembl
chr1:14619223..14622441hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383219
hg193219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427741
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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