A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205579



Internal ID20772619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157445477..157454122hg38UCSC Ensembl
chr2:158301989..158310634hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg388646
hg198646
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205579
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00066


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