A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529972



Internal ID21854328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231167319..231167627hg38UCSC Ensembl
chr1:231303065..231303373hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982861
Supporting Variants
Samples
Known GenesTRIM67
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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