A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206302



Internal ID20773342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55779710..55797212hg38UCSC Ensembl
chr2:56006845..56024347hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3817503
hg1917503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206302
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