A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854544



Internal ID22629479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42947512..42956441hg38UCSC Ensembl
chr8:42802655..42811584hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388930
hg198930
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506665
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854544
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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