A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445421



Internal ID21102974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93699601..93705600hg38UCSC Ensembl
chr10:95459358..95465357hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189255
Samples
Known GenesFRA10AC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445421
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