A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902330



Internal ID2357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22264065..22265453hg38UCSC Ensembl
chr1:22590558..22591946hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902330
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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