A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484355



Internal ID21141908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50953718..50954074hg38UCSC Ensembl
chr13:51527854..51528210hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009646
Samples
Known GenesRNASEH2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484355
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