A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350611



Internal ID21008164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32288794..32374707hg38UCSC Ensembl
chr2:32513863..32599775hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3885914
hg1985913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3823n223
Supporting Variantsnssv18208204
Samples
Known GenesBIRC6, YIPF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350611
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