A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495578



Internal ID21153131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105193104..105193530hg38UCSC Ensembl
chr13:105845455..105845881hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495578
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