A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206381



Internal ID20773421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62272194..62273216hg38UCSC Ensembl
chr2:62499329..62500351hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206381
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