A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399088



Internal ID21056641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256601..384500hg38UCSC Ensembl
chr6:256601..384500hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127900
hg19127900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6038n223
Supporting Variantsnssv18234996
Samples
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399088
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