A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495478



Internal ID21153031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112603701..112608900hg38UCSC Ensembl
chr13:113258015..113263214hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495478
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