A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864887



Internal ID22639822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65432612..65437612hg38UCSC Ensembl
chr8:66344847..66349847hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2015n209
Supporting Variantsnssv17509685, nssv17509686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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