A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445680



Internal ID21103233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70240835..70305787hg38UCSC Ensembl
chr10:72000591..72065543hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3864953
hg1964953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186995
Samples
Known GenesLRRC20, NPFFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445680
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