A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339303



Internal ID20996856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64057697..64059369hg38UCSC Ensembl
chr2:64284831..64286503hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339303
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