A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029368



Internal ID21938711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1620775..1620988hg38UCSC Ensembl
chr12:1729941..1730154hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608378
Samples
Known GenesWNT5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer