A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984852



Internal ID20551893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88192801..88214200hg38UCSC Ensembl
chr10:89952558..89973957hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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