A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926899



Internal ID22702127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115643579..115647086hg38UCSC Ensembl
chr11:115514297..115517804hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383508
hg193508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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