A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754057



Internal ID21385227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167126818..167131494hg38UCSC Ensembl
chr3:166844606..166849282hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384677
hg194677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433939
Supporting Variants
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754057
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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