A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877759



Internal ID22652724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40355355..40358379hg38UCSC Ensembl
chr19:40861262..40864286hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383025
hg193025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475394
Samples
Known GenesPLD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877759
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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