A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944017



Internal ID22719475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10385074..10385963hg38UCSC Ensembl
chr19:10495750..10496639hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392109
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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