A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587396



Internal ID21779439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26586807..26589289hg38UCSC Ensembl
chr11:26608354..26610836hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382483
hg192483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020693
Supporting Variants
Samples
Known GenesANO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587396
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