A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892258



Internal ID169030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175062390..175145269hg38UCSC Ensembl
chr1:175031526..175114405hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3882880
hg1982880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430749
Supporting Variants
Samples
Known GenesTNN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892258
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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