A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514681



Internal ID22572639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88415720..88424174hg38UCSC Ensembl
chr9:91030635..91039089hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg388455
hg198455
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848790
Supporting Variants
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514681
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