A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343038



Internal ID21000591
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 StatusM
Merged Variants
Supporting Variantsnssv18205579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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