A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946986



Internal ID22722486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39435314..39435390hg38UCSC Ensembl
chr19:39925954..39926030hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408735
Samples
Known GenesRPS16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946986
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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