A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411802



Internal ID21069355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87486902..87488275hg38UCSC Ensembl
chr6:88196620..88197993hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149098
Samples
Known GenesSLC35A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411802
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