A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173479



Internal ID20740519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92742744..92743608hg38UCSC Ensembl
chr8:93754972..93755836hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420775
Supporting Variants
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173479
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