A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981835



Internal ID21891178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172946635..173165928hg38UCSC Ensembl
chr1:172915775..173135067hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38219294
hg19219293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531123
Samples
Known GenesTNFSF18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981835
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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