A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512578



Internal ID22570532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2745606..2746855hg38UCSC Ensembl
chr9:2745606..2746855hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512578
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