A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486738



Internal ID21144291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103352354..103397844hg38UCSC Ensembl
chr13:104004704..104050194hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3845491
hg1945491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486738
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