A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398358



Internal ID21055911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28700841..28726700hg38UCSC Ensembl
chr6:28668618..28694477hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3825860
hg1925860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398358
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