A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885692



Internal ID22660678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39103886..39113529hg38UCSC Ensembl
chr19:39594526..39604169hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg389644
hg199644
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475375
Samples
Known GenesPAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885692
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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