A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367411



Internal ID22593080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20583105..20584839hg38UCSC Ensembl
chr11:20604651..20606385hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367411
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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