A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854769



Internal ID22629704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69356052..69357779hg38UCSC Ensembl
chr8:70268287..70270014hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381728
hg191728
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509759, nssv17509758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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