A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514774



Internal ID22572733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93159187..93163925hg38UCSC Ensembl
chr9:95921469..95926207hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384739
hg194739
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514774
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