A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855585



Internal ID22630520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115867343..115871920hg38UCSC Ensembl
chr8:116879569..116884146hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384578
hg194578
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855585
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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