A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165199



Internal ID20732239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15268085..17187766hg38UCSC Ensembl
chr8:15125594..17045275hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381919682
hg191919682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416566
Supporting Variants
Samples
Known GenesFGF20, MICU3, MSR1, TUSC3, ZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165199
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