A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940753



Internal ID22716166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15212215..15213341hg38UCSC Ensembl
chr19:15323026..15324152hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1015n209
Supporting Variantsnssv17407016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940753
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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