A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891672



Internal ID168639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173203011..173203053hg38UCSC Ensembl
chr1:173172150..173172192hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544561
Supporting Variants
Samples
Known GenesTNFSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891672
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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