A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416262



Internal ID195494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96609464..96656561hg38UCSC Ensembl
chr1:97075020..97122117hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3847098
hg1947098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416262
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer