A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv362n172



Internal ID22814736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9819399..9820760hg38UCSC Ensembl
chr19:9930075..9931436hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381362
hg191362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432904, nsv4432903
SamplesNB08, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv362n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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