A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916116



Internal ID22691335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45734283..45735219hg38UCSC Ensembl
chr11:45755834..45756770hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916116
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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