A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364883



Internal ID21022436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55466334..55466927hg38UCSC Ensembl
chr3:55500362..55500955hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210030
Samples
Known GenesWNT5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364883
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