A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617186



Internal ID20990257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121405640..121410143hg38UCSC Ensembl
chr6:121726786..121731289hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384504
hg194504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6380n223
Supporting Variantsnssv18137543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617186
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