A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354677



Internal ID22580346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76801870..76805467hg38UCSC Ensembl
chr11:76512914..76516511hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383598
hg193598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354677
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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