A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486741



Internal ID21144294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83902901..83912900hg38UCSC Ensembl
chr13:84477036..84487035hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486741
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