A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354760



Internal ID21012313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47393464..47400566hg38UCSC Ensembl
chr2:47620603..47627705hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg387103
hg197103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354760
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