A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902096



Internal ID2194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41278200..41278837hg38UCSC Ensembl
chr1:41743872..41744509hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.066032


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