A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398324



Internal ID21055877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29893532..29948271hg38UCSC Ensembl
chr6:29861309..29916048hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854740
hg1954740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6117n223
Supporting Variantsnssv18141403
Samples
Known GenesHCG4B, HLA-A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398324
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