A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437465



Internal ID21095018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98383407..98388171hg38UCSC Ensembl
chr10:100143164..100147928hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384765
hg194765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196036
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437465
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