A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933811



Internal ID21353880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82418930..82419272hg38UCSC Ensembl
chr9:85033845..85034187hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198962
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933811
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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