A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004341



Internal ID21913684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121283153..121283229hg38UCSC Ensembl
chr9:124045431..124045507hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579396
Samples
Known GenesGSN, GSN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004341
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