A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862115



Internal ID22637050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89395523..89426206hg38UCSC Ensembl
chr11:89128691..89159374hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3830684
hg1930684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462150, nssv17454338
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862115
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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