A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464455



Internal ID22522342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102846465..102847464hg38UCSC Ensembl
chr10:104606222..104607221hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464455
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