A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494687



Internal ID21152240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58753601..58757100hg38UCSC Ensembl
chr13:59327735..59331234hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494687
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