A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027199



Internal ID21936542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71332326..71378537hg38UCSC Ensembl
chr15:71624665..71670876hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3846212
hg1946212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606553
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027199
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