A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908182



Internal ID22683392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17195287..17201372hg38UCSC Ensembl
chr11:17216834..17222919hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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