A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207605



Internal ID20774645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:125429159..125430063hg38UCSC Ensembl
chr2:126186736..126187640hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer