A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343761



Internal ID21001314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192845675..193056441hg38UCSC Ensembl
chr2:193710401..193921167hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38210767
hg19210767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343761
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