A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523358



Internal ID20896719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11147054..11151370hg38UCSC Ensembl
chr20:11127702..11132018hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384317
hg194317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523358
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