A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939548



Internal ID22714943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35028834..35029123hg38UCSC Ensembl
chr19:35519738..35520027hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939548
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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