A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920877



Internal ID22696100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78772635..78772693hg38UCSC Ensembl
chr11:78483680..78483738hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363249
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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