A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934176



Internal ID22709497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46761163..46765584hg38UCSC Ensembl
chr19:47264420..47268841hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934176
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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