A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227965



Internal ID20795005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55614010..55734005hg38UCSC Ensembl
chr8:56526569..56646564hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38119996
hg19119996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227965
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