A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609055



Internal ID20982126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104884858..104886453hg38UCSC Ensembl
chr6:105332733..105334328hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381596
hg191596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609055
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