A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733627



Internal ID20509557
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 StatusM
Merged Variants
Supporting Variantsnssv16292025
Samples
Known GenesCHCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733627
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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