A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891093



Internal ID168239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160823387..160825342hg38UCSC Ensembl
chr1:160793177..160795132hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381956
hg191956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432223
Supporting Variants
Samples
Known GenesLY9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891093
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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