A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946619



Internal ID22722112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52259521..52268270hg38UCSC Ensembl
chr19:52762774..52771523hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg388750
hg198750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946619
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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