A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005814



Internal ID21915157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138234775..138234829hg38UCSC Ensembl
chr9:141125225..141125279hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589156
Samples
Known GenesFAM157B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005814
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