A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707036



Internal ID21379312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14119423..14119496hg38UCSC Ensembl
chr3:14160923..14160996hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390350
Supporting Variants
Samples
Known GenesCHCHD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707036
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.255747


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