A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882278



Internal ID22657255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58509077..58516065hg38UCSC Ensembl
chr19:59020444..59027432hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386989
hg196989
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479348
Samples
Known GenesSLC27A5, ZBTB45
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882278
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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