A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859625



Internal ID22634560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96818228..96826634hg38UCSC Ensembl
chr9:99580510..99588916hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514932
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859625
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