A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403799



Internal ID21061352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56692101..56929300hg38UCSC Ensembl
chr6:56556899..56794098hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38237200
hg19237200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226057
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer