A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859039



Internal ID22633974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38548422..38549800hg38UCSC Ensembl
chr8:38405940..38407318hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381379
hg191379
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859039
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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