A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487364



Internal ID21144917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109819628..109819973hg38UCSC Ensembl
chr13:110471975..110472320hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487364
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