A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979508



Internal ID20546548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110472900..110495542hg38UCSC Ensembl
chr10:112232658..112255300hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3822643
hg1922643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442878
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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