A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485401



Internal ID21142954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68860901..68863500hg38UCSC Ensembl
chr13:69435033..69437632hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012166
Samples
Known GenesLINC00550
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485401
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