A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165861



Internal ID20732901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30697860..30950805hg38UCSC Ensembl
chr8:30555377..30808321hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38252946
hg19252945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422517
Supporting Variants
Samples
Known GenesGSR, PPP2CB, TEX15, UBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165861
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