A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853663



Internal ID22628598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128012758..128018807hg38UCSC Ensembl
chr9:130775037..130781086hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386050
hg196050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2194n209
Supporting Variantsnssv17511412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853663
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