A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083736



Internal ID20650776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223851924..223859966hg38UCSC Ensembl
chr2:224716641..224724683hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg388043
hg198043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083736
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