A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432834



Internal ID21394836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4616501..4621473hg38UCSC Ensembl
chr19:4616513..4621485hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384973
hg194973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv356n172
Supporting Variantsnssv15750163
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432834
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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