A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886790



Internal ID22661779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18656835..18662834hg38UCSC Ensembl
chr19:18767645..18773644hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473858
Samples
Known GenesKLHL26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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