A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605262



Internal ID21797309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132048415..132048415hg38UCSC Ensembl
chr11:131918309..131918309hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091241
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605262
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