A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167418



Internal ID20734458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35610509..35616819hg38UCSC Ensembl
chr8:35468027..35474337hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433365
Supporting Variants
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167418
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