A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440953



Internal ID21098506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103292613..103305838hg38UCSC Ensembl
chr10:105052370..105065595hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3813226
hg1913226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194228
Samples
Known GenesPCGF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440953
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