A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931122



Internal ID22706401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31893530..31893625hg38UCSC Ensembl
chr19:32384436..32384531hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931122
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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