A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168699



Internal ID20735739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60945301..60956100hg38UCSC Ensembl
chr8:61857860..61868659hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00164


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