A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173836



Internal ID20740876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98107915..98114435hg38UCSC Ensembl
chr8:99120143..99126663hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433382
Supporting Variants
Samples
Known GenesHRSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173836
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