A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv356n172



Internal ID22814730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4616497..4621707hg38UCSC Ensembl
chr19:4616509..4621719hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432833, nsv4432834
SamplesNB12, NB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv356n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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