A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227288



Internal ID20794328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76942155..76970444hg38UCSC Ensembl
chr8:77854391..77882680hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3828290
hg1928290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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