A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861019



Internal ID22635954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42920288..42938555hg38UCSC Ensembl
chr8:42775431..42793698hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3818268
hg1918268
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506662
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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