A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851036



Internal ID22625971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39649598..39651877hg38UCSC Ensembl
chr8:39507117..39509396hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382280
hg192280
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506079
Samples
Known GenesADAM18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer