A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192723



Internal ID20759763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117449154..117482723hg38UCSC Ensembl
chr10:119208665..119242234hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3833570
hg1933570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192723
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