A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984811



Internal ID20551852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87747629..87749576hg38UCSC Ensembl
chr10:89507386..89509333hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381948
hg191948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442243
Supporting Variants
Samples
Known GenesPAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00118


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