A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514671



Internal ID22572629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88395021..88398220hg38UCSC Ensembl
chr9:91009936..91013135hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856193
Supporting Variants
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514671
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