A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417890



Internal ID197075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39051471..39062983hg38UCSC Ensembl
chr1:39517143..39528655hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3811513
hg1911513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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