A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364197



Internal ID22589866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71387760..71387862hg38UCSC Ensembl
chr11:71098806..71098908hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364197
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014


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