A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921309



Internal ID22696532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78796091..78804230hg38UCSC Ensembl
chr11:78507136..78515275hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388140
hg198140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353104
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921309
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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