A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352508



Internal ID22578177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87438810..87438810hg38UCSC Ensembl
chr11:87149852..87149852hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977652
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352508
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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