A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218534



Internal ID20785574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98059681..98065693hg38UCSC Ensembl
chr7:97688993..97695005hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg386013
hg196013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218534
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