A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929390



Internal ID22704643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48632328..48632454hg38UCSC Ensembl
chr19:49135585..49135711hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397601
Samples
Known GenesDBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929390
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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