A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433939



Internal ID21395941
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 StatusM
Merged Variantsdgv536n172
Supporting Variantsnssv15750224, nssv15754057, nssv15750995
SamplesBTQ038, BTQ055, NB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433939
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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