A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913739



Internal ID22688955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76841716..76841799hg38UCSC Ensembl
chr11:76552760..76552843hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913739
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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