A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886057



Internal ID22661043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58363458..58370719hg38UCSC Ensembl
chr19:58874825..58882086hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg387262
hg197262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479335
Samples
Known GenesZNF837
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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