A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190546



Internal ID20757586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124034519..124035353hg38UCSC Ensembl
chr10:125794035..125794869hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442618
Supporting Variants
Samples
Known GenesCHST15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer