A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034045



Internal ID21943388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44724662..44726030hg38UCSC Ensembl
chr17:42802030..42803398hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633377
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034045
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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