A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745934



Internal ID20521945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14119424..14119498hg38UCSC Ensembl
chr3:14160924..14160998hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265202
Samples
Known GenesCHCHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745934
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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