A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281863



Internal ID20491081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73871654..73873714hg38UCSC Ensembl
chr9:76486570..76488630hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382061
hg192061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735168
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281863
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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