A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867482



Internal ID22642417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65432613..65438599hg38UCSC Ensembl
chr8:66344848..66350834hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385987
hg195987
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2015n209
Supporting Variantsnssv17509687, nssv17509688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867482
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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