A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486816



Internal ID21144369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35728103..35732173hg38UCSC Ensembl
chr13:36302240..36306310hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179040
Samples
Known GenesMIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486816
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