A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481185



Internal ID21138738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106403999..106404398hg38UCSC Ensembl
chr13:107056347..107056746hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481185
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