A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351069



Internal ID22576738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38577781..38577965hg38UCSC Ensembl
chr11:38599331..38599515hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351069
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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