A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592117



Internal ID21784160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59775784..59786384hg38UCSC Ensembl
chr11:59543257..59553857hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3810601
hg1910601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033573
Supporting Variants
Samples
Known GenesSTX3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592117
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