A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003564



Internal ID21912907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119221375..119223861hg38UCSC Ensembl
chr9:121983653..121986139hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382487
hg192487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587419
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003564
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