A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363485



Internal ID21021038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14059638..14063628hg38UCSC Ensembl
chr3:14101138..14105128hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg383991
hg193991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094007
Samples
Known GenesTPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363485
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