A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365549



Internal ID21023102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143839517..143899064hg38UCSC Ensembl
chr3:143558359..143617906hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3859548
hg1959548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209675
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365549
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