A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921427



Internal ID22696651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79192073..79192123hg38UCSC Ensembl
chr11:78903118..78903168hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367668
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921427
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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