A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904492



Internal ID3815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64373817..64386000hg38UCSC Ensembl
chr1:64839500..64851683hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3812184
hg1912184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.030056


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