A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981029



Internal ID20548069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18812797..18821930hg38UCSC Ensembl
chr10:19101726..19110859hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389134
hg199134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981029
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