A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855754



Internal ID22630689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48962350..48968124hg38UCSC Ensembl
chr8:49874909..49880683hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg385775
hg195775
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855754
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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