A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924214



Internal ID22699441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116229880..116241204hg38UCSC Ensembl
chr11:116100597..116111921hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811325
hg1911325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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