A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491389



Internal ID21148942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101452720..101638270hg38UCSC Ensembl
chr13:102105071..102290620hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38185551
hg19185550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182034
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491389
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