A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425057



Internal ID21082610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23773947..23775335hg38UCSC Ensembl
chr9:23773945..23775333hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191698
Samples
Known GenesELAVL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425057
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