A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586983



Internal ID21779026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74090498..74090498hg38UCSC Ensembl
chr11:73801543..73801543hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088783
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586983
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