A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514528



Internal ID22572486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85646492..85658089hg38UCSC Ensembl
chr9:88261407..88273004hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3811598
hg1911598
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856971
Supporting Variants
Samples
Known GenesAGTPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514528
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