A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292025



Internal ID20501243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126924626..126934286hg38UCSC Ensembl
chr3:126643469..126653129hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg389661
hg199661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733627
Supporting Variants
Samples
Known GenesCHCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292025
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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