A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489086



Internal ID21146639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35932470..35934376hg38UCSC Ensembl
chr13:36506607..36508513hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381907
hg191907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008975
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489086
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