A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345914



Internal ID21003467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:198510901..198512400hg38UCSC Ensembl
chr2:199375625..199377124hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4252n223
Supporting Variantsnssv18084303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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