A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981666



Internal ID20548706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43687227..43691682hg38UCSC Ensembl
chr10:44182675..44187130hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384456
hg194456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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