A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482671



Internal ID21140224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68387766..68398538hg38UCSC Ensembl
chr14:68854483..68865255hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3810773
hg1910773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020566
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer