A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487821



Internal ID21145374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109766801..109908600hg38UCSC Ensembl
chr13:110419148..110560947hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38141800
hg19141800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190381
Samples
Known GenesIRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer