A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401811



Internal ID21059364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96048603..96049052hg38UCSC Ensembl
chr6:96496479..96496928hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149865
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401811
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