A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882280



Internal ID22657257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39070231..39086376hg38UCSC Ensembl
chr19:39560871..39577016hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816146
hg1916146
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475370
Samples
Known GenesPAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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