A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587744



Internal ID21779787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62730359..62732284hg38UCSC Ensembl
chr11:62497831..62499756hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381926
hg191926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039864
Supporting Variants
Samples
Known GenesTTC9C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587744
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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