A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017194



Internal ID21926537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96157781..96157858hg38UCSC Ensembl
chr9:98920063..98920140hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017194
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