A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911987



Internal ID22687202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78827348..78827418hg38UCSC Ensembl
chr11:78538393..78538463hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365396
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911987
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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