A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399780



Internal ID21057333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89911631..89913324hg38UCSC Ensembl
chr6:90621350..90623043hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381694
hg191694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399780
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