A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165876



Internal ID20732916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30841401..30846400hg38UCSC Ensembl
chr8:30698917..30703916hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429723
Supporting Variants
Samples
Known GenesTEX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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