A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854962



Internal ID22629897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114248746..114250051hg38UCSC Ensembl
chr11:114119468..114120773hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454580, nssv17468283
Samples
Known GenesZBTB16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854962
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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