A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892156



Internal ID168960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169914117..169919041hg38UCSC Ensembl
chr1:169883258..169888182hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg384925
hg194925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892156
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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